Acetaminophen And Codeine


Proficient Rx Lp
Human Prescription Drug
NDC 63187-491
Acetaminophen And Codeine is a human prescription drug labeled by 'Proficient Rx Lp'. National Drug Code (NDC) number for Acetaminophen And Codeine is 63187-491. This drug is available in dosage form of Tablet. The names of the active, medicinal ingredients in Acetaminophen And Codeine drug includes Acetaminophen - 300 mg/1 Codeine Phosphate - 30 mg/1 . The currest status of Acetaminophen And Codeine drug is Active.

Drug Information:

Drug NDC: 63187-491
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Acetaminophen And Codeine
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Acetaminophen And Codeine
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Proficient Rx Lp
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Tablet
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:ACETAMINOPHEN - 300 mg/1
CODEINE PHOSPHATE - 30 mg/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: ANDA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 29 May, 2008
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 21 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: ANDA040779
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Proficient Rx LP
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:993781
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
UNII:362O9ITL9D
GSL05Y1MN6
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class:Full Opioid Agonists [MoA]
Opioid Agonist [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.
DEA Schedule:CIII
This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
63187-491-2020 TABLET in 1 BOTTLE (63187-491-20)02 Feb, 2015N/ANo
63187-491-3030 TABLET in 1 BOTTLE (63187-491-30)02 Feb, 2015N/ANo
63187-491-6060 TABLET in 1 BOTTLE (63187-491-60)02 Feb, 2015N/ANo
63187-491-9090 TABLET in 1 BOTTLE (63187-491-90)02 Feb, 2015N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Acetaminophen and codeine acetaminophen and codeine acetaminophen acetaminophen codeine phosphate codeine anhydrous croscarmellose sodium crospovidone (15 mpa.s at 5%) lactose monohydrate magnesium stearate microcrystalline cellulose povidone, unspecified starch, corn stearic acid ip33;3

Boxed Warning:

Warning: death related to ultra-rapid metabolism of codeine to morphine respiratory depression and death have occurred in children who received codeine following tonsillectomy and/or adenoidectomy and had evidence of being ultra-rapid metabolizers of codeine due to a cyp2d6 polymorphism. hepatotoxicity acetaminophen has been associated with cases of acute liver failure, at times resulting in liver transplant and death. most of the cases of liver injury are associated with the use of acetaminophen at doses that exceed 4000 milligrams per day, and often involve more than one acetaminophen-containing product.

Indications and Usage:

1 indications and usage acetaminophen and codeine phosphate tablets, usp are indicated for the relief of mild to moderately severe pain.

Warnings:

Warnings hepatotoxicity acetaminophen has been associated with cases of acute liver failure, at times resulting in liver transplant and death. most of the cases of liver injury are associated with the use of acetaminophen at doses that exceed 4000 milligrams per day, and often involve more than one acetaminophen-containing product. the excessive intake of acetaminophen may be intentional to cause self-harm or unintentional as patients attempt to obtain more pain relief or unknowingly take other acetaminophen-containing products. the risk of acute liver failure is higher in individuals with underlying liver disease and in individuals who ingest alcohol while taking acetaminophen. instruct patients to look for acetaminophen or apap on package labels and not to use more than one product that contains acetaminophen. instruct patients to seek medical attention immediately upon ingestion of more than 4000 milligrams of acetaminophen per day, even if they feel well. serious skin reactions rar
ely, acetaminophen may cause serious skin reactions such as acute generalized exanthematous pustulosis (agep), stevens-johnson syndrome (sjs), and toxic epidermal necrolysis (ten), which can be fatal. patients should be informed about the signs of serious skin reactions, and use of the drug should be discontinued at the first appearance of skin rash or any other sign of hypersensitivity. death related to ultra-rapid metabolism of codeine to morphine respiratory depression and death have occurred in children who received codeine in the post-operative period following tonsillectomy and/or adenoidectomy and had evidence of being ultra-rapid metabolizers of codeine (i.e., multiple copies of the gene for cytochrome p450 isoenzyme 2d6 of high morphine concentrations). deaths have also occurred in nursing infants who were exposed to high levels of morphine in breast milk because their mothers were ultra-rapid metabolizers of codeine [see precautions, nursing mothers ]. some individuals may be ultra-rapid metabolizers because of a specific cyp2d6 genotype (gene duplications denoted as *1/*1xn or *1/*2xn). the prevalence of this cyp2d6 phenotype varies widely and has been estimated at 0.5 to 1% in chinese and japanese, 0.5 to 1% in hispanics, 1 to 10% in caucasians, 3% in african americans, and 16 to 28% in north africans, ethiopians and arabs. data are not available for other ethnic groups. these individuals convert codeine into its active metabolite, morphine, more rapidly and completely than other people. this rapid conversion results in higher than expected serum morphine levels. even at labeled dosage regimens, individuals who are ultra-rapid metabolizers may have life-threatening or fatal respiratory depression or experience signs of overdose (such as extreme sleepiness, confusion, or shallow breathing) [see overdosage ]. children with obstructive sleep apnea who are treated with codeine for post-tonsillectomy and/or adenoidectomy pain may be particularly sensitive to the respiratory depressant effects of codeine that has been rapidly metabolized to morphine. codeine-containing products are contraindicated for post-operative pain management in all pediatric patients undergoing tonsillectomy and/or adenoidectomy [see contraindications ]. when prescribing codeine-containing products, healthcare providers should choose the lowest effective dose for the shortest period of time and inform patients and caregivers about these risks and the signs of morphine overdose [see overdosage ]. hypersensitivity/ anaphylaxis there have been post-marketing reports of hypersensitivity and anaphylaxis associated with use of acetaminophen. clinical signs include swelling of the face, mouth and throat, respiratory distress, urticaria, rash, pruritus and vomiting. there were infrequent reports of life-threatening anaphylaxis requiring emergency medical attention. instruct patients to discontinue acetaminophen and codeine phosphate tablets, usp immediately and seek medical care if they experience these symptoms. do not prescribe acetaminophen and codeine phosphate tablets, usp for patients with acetaminophen allergy. in the presence of head injury or other intracranial lesions, the respiratory depressant effects of codeine and other narcotics may be markedly enhanced, as well as their capacity for elevating cerebrospinal fluid pressure. narcotics also produce other cns depressant effects, such as drowsiness, that may further obscure the clinical course of the patients with head injuries. codeine or other narcotics may obscure signs on which to judge the diagnosis or clinical course of patients with acute abdominal conditions. codeine is habit forming and potentially abusable. consequently, the extended use of this product is not recommended.

Warnings and Cautions:

5 warnings and precautions click here to enter warnings and precautions

Dosage and Administration:

2 dosage and administration dosage should be adjusted according to severity of pain and response of the patient. the usual adult dosage is: single doses maximum range 24-hour dose codeine phosphate 15mg to 60mg 360 mg acetaminophen 300 mg to 1000 mg 4000 mg the usual dose of codeine phosphate in children is 0.5 mg/kg. doses may be repeated up to every 4 hours. the prescriber must determine the number of tablets per dose, and the maximum number of tablets per 24 hours, based upon the above dosage guidance. this information should be conveyed in the prescription. it should be kept in mind, however, that tolerance to codeine can develop with continued use and that the incidence of untoward effects is dose related. adult doses of codeine higher than 60 mg fail to give commensurate relief of pain but merely prolong analgesia and are associated with an appreciably increased incidence of undesirable side effects. equivalently high doses in children would have similar effects.

Dosage Forms and Strength:

3 dosage forms and strengths click here to enter dosage forms and strengths

Contraindications:

4 contraindications codeine-containing products are contraindicated for post-operative pain management in children who have undergone tonsillectomy and/or adenoidectomy. acetaminophen and codeine phosphate tablets should not be administered to patients who have previously exhibited hypersensitivity to codeine or acetaminophen.

Adverse Reactions:

6 adverse reactions the most frequently observed adverse reactions include drowsiness, lightheadedness, dizziness, sedation, shortness of breath, nausea and vomiting. these effects seem to be more prominent in ambulatory than in non-ambulatory patients, and some of these adverse reactions may be alleviated if the patient lies down. other adverse reactions include allergic reactions, euphoria, dysphoria, constipation, abdominal pain, pruritus, rash, thrombocytopenia and agranulocytosis. at higher doses codeine has most of the disadvantages of morphine including respiratory depression.

Use in Specific Population:

8 use in specific populations click here to enter use in specific populations 8.1 pregnancy click here to enter pregnancy 8.2 lactation click here to enter lactation 8.3 females and males of reproductive potential click here to enter females and males of reproductive potential 8.4 pediatric use click here to enter pediatric use 8.5 geriatric use click here to enter geriatric use

Use in Pregnancy:

8.1 pregnancy click here to enter pregnancy

Pediatric Use:

8.4 pediatric use click here to enter pediatric use

Geriatric Use:

8.5 geriatric use click here to enter geriatric use

Overdosage:

10 overdosage following an acute overdosage, toxicity may result from codeine or acetaminophen. signs and symptoms: toxicity from codeine poisoning includes the opioid triad of: pinpoint pupils, depression of respiration and loss of consciousness. convulsions may occur. in acetaminophen overdosage: dose-dependent, potentially fatal hepatic necrosis is the most serious adverse effect. renal tubular necrosis, hypoglycemic coma and coagulation defects may also occur. early symptoms following a potentially hepatotoxic overdose may include: nausea, vomiting, diaphoresis and general malaise. clinical and laboratory evidence of hepatic toxicity may not be apparent until 48 to 72 hours post-ingestion. treatment: a single or multiple drug overdose with acetaminophen and codeine is a potentially lethal polydrug overdose, and consultation with a regional poison control center is recommended. immediate treatment includes support of cardiorespiratory function and measures to reduce drug absorption. oxygen, intravenous fluids, vasopressors and other supportive measures should be employed as indicated. assisted or controlled ventilation should also be considered. for respiratory depression due to overdosage or unusual sensitivity to codeine phosphate, parenteral naloxone is a specific and effective antagonist. gastric decontamination with activated charcoal should be administered just prior to n-acetylcysteine (nac) to decrease systemic absorption if acetaminophen ingestion is known or suspected to have occurred within a few hours of presentation. serum acetaminophen levels should be obtained immediately if the patient presents 4 hours or more after ingestion to assess potential risk of hepatotoxicity; acetaminophen levels drawn less then 4 hours post-ingestion may be misleading. to obtain the best possible outcome, nac should be administered as soon as possible where impending or evolving liver injury is suspected. intravenous nac may be administered when circumstances preclude oral administration. vigorous supportive therapy is required in severe intoxication. procedures to limit the continuing absorption of the drug must be readily performed since the hepatic injury is dose dependent and occurs early in the course of intoxication.

dependence:

9.3 dependence click here to enter dependence

Description:

11 description each tablet contains: acetaminophen, usp……………………………………………………..300 mg codeine phosphate, usp…………………………………………………...30 mg (warning: may be habit forming) inactive ingredients: croscarmellose sodium, crospovidone, lactose monohydrate, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch and stearic acid. acetaminophen and codeine is supplied in tablet form for oral administration. acetaminophen, 4'-hydroxyacetanlllde, is a slightly bitter, white, odorless, crystalline powder, is a non-opiate, non-salicylate analgesic and antipyretic. it has the following structural formula: codeine phosphate: 7,8-didehydro-4,5α-epoxy-3-methoxy-l7-methylmorphinan-6α-ol phosphate (1:1) (salt) hemihydrate, a white crystalline powder, is a narcotic analgesic and antitussive. it has the following structural formula: 9ba1db7f-figure-01 9ba1db7f-figure-02

Clinical Pharmacology:

12 clinical pharmacology acetaminophen and codeine phosphate tablets combines the analgesic effects of a centrally acting analgesic, codeine, with a peripherally acting analgesic, acetaminophen. pharmacokinetics the behavior on the individual components is described below. codeine codeine is rapidly absorbed from the gastrointestinal tract. it is rapidly distributed from the intravascular spaces to the various body tissues, with preferential uptake by parenchymatous organs such as the liver, spleen and kidney. codeine crosses the blood-brain barrier, and is found in fetal tissue and breast milk. the plasma concentration does not correlate with brain concentration or relief of pain: however, codeine is not bound to plasma proteins and does not accumulate in body tissues. the plasma half-life is about 2.9 hours. the elimination of codeine is primarily via the kidneys, and about 90% of an oral dose is excreted by the kidneys within 24 hours of dosing. the urinary secretion products consis
t of free and glucuronide (about 70%). free and conjugated morphine (about 10%), normorphine (4%) and hydrocodone (1%). the remainder of the dose is excreted in the feces. at therapeutic doses, the analgesic effect reaches a peak within 2 hours and persists between 4 and 6 hours. see overdosage for toxicity information. acetaminophen acetaminophen is rapidly absorbed from the gastrointestinal tract and is distributed throughout most body tissues. the plasma half-life is 1.25 to 3 hours, but may be increased by liver damage and following overdosage. elimination of acetaminophen is principally by liver metabolism (conjugation) and subsequent renal excretion of metabolites. approximately 85% of an oral dose appears in the urine within 24 hours of administration, most as the glucuronide conjugate, with small amounts of other conjugates and unchanged drug. see overdosage for toxicity information. 12.1 mechanism of action click here to enter mechanism of action 12.2 pharmacodynamics click here to enter pharmacodynamics 12.3 pharmacokinetics click here to enter pharmacokinetics

Mechanism of Action:

12.1 mechanism of action click here to enter mechanism of action

Pharmacodynamics:

12.2 pharmacodynamics click here to enter pharmacodynamics

Pharmacokinetics:

12.3 pharmacokinetics click here to enter pharmacokinetics

Nonclinical Toxicology:

13 nonclinical toxicology click here to enter nonclinical toxicology 13.1 carcinogenesis, mutagenesis, impairment of fertility click here to enter carcinogenesis, mutagenesis, impairment of fertility 13.2 animal toxicology and/or pharmacology click here to enter animal toxicology and/or pharmacology

Carcinogenesis and Mutagenesis and Impairment of Fertility:

13.1 carcinogenesis, mutagenesis, impairment of fertility click here to enter carcinogenesis, mutagenesis, impairment of fertility

Clinical Studies:

14 clinical studies click here to enter clinical studies

How Supplied:

16 how supplied/storage and handling acetaminophen and codeine phosphate tablets, usp 300 mg /30 mg are white, round, flat, beveled edged tablets debossed “ip 33” on obverse and “3” on reverse. they are available as follows: bottles of 20: ndc 63187-491-20 bottles of 30: ndc 63187-491-30 bottles of 60 : ndc 63187-491-60 bottles of 90 : ndc 63187-491-90 store acetaminophen and codeine phosphate tablets, usp 300 mg/30 mg at 20° to 25°c (68° to 77°f) [see usp controlled room temperature]. dispense in tight, light-resistant container as defined in the usp. questions or comments? call 1-877-835-5472 monday through friday 9am-5pm est manufactured by: amneal pharmaceuticals hauppauge, ny 11788 repackaged by: proficient rx lp thousand oaks, ca 91320 rev. 10-2013

Information for Patients:

17 patient counseling information click here to enter patient counseling information

Package Label Principal Display Panel:

Package/label principal display panel 63187-491-30


Comments/ Reviews:

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