Methylergonovine Maleate


Hf Acquisition Co Llc, Dba Healthfirst
Human Prescription Drug
NDC 51662-1556
Methylergonovine Maleate is a human prescription drug labeled by 'Hf Acquisition Co Llc, Dba Healthfirst'. National Drug Code (NDC) number for Methylergonovine Maleate is 51662-1556. This drug is available in dosage form of Injection. The names of the active, medicinal ingredients in Methylergonovine Maleate drug includes Methylergonovine Maleate - .2 mg/mL . The currest status of Methylergonovine Maleate drug is Active.

Drug Information:

Drug NDC: 51662-1556
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: Methylergonovine Maleate
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: Methylergonovine Maleate
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Hf Acquisition Co Llc, Dba Healthfirst
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Injection
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:METHYLERGONOVINE MALEATE - .2 mg/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:INTRAVENOUS
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: 14 Jun, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 17 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: ANDA040889
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:HF Acquisition Co LLC, DBA HealthFirst
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:996828
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:IR84JPZ1RK
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:Ergolines [CS]
Ergot Derivative [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
51662-1556-11 mL in 1 AMPULE (51662-1556-1)14 Jun, 2021N/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:

Methylergonovine maleate methylergonovine maleate maleic acid sodium chloride methylergonovine maleate methylergonovine water

Indications and Usage:

Indications & usage following delivery of the placenta, for routine management of uterine atony, hemorrhage and subinvolution of the uterus. for control of uterine hemorrhage in the second stage of labor following delivery of the anterior shoulder.

Warnings:

Warnings general this drug should not be administered i.v. routinely because of the possibility of inducing sudden hypertensive and cerebrovascular accidents. if i.v. administration is considered essential as a lifesaving measure, methylergonovine maleate should be given slowly over a period of no less than 60 seconds with careful monitoring of blood pressure. intra-arterial or periarterial injection should be strictly avoided. caution should be exercised in the presence of impaired hepatic or renal function. breast-feeding mothers should not breast-feed during treatment with methylergonovine maleate injection. milk secreted during this period should be discarded. methylergonovine maleate injection may produce adverse effects in the breast-feeding infant. methylergonovine maleate injection may also reduce the yield of breast milk. mothers should wait at least 12 hours after administration of the last dose of methylergonovine maleate injection before initiating or resuming breast-feedin
g. coronary artery disease patients with coronary artery disease or risk factors for coronary artery disease (e.g., smoking, obesity, diabetes, high cholesterol) may be more susceptible to developing myocardial ischemia and infarction associated with methylergonovine-induced vasospasm. medication errors inadvertent administration of methylergonovine maleate injection to newborn infants has been reported. in these cases of inadvertent neonatal exposure, symptoms such as respiratory depression, convulsions, cyanosis and oliguria have been reported. usual treatment is symptomatic. however, in severe cases, respiratory and cardiovascular support is required. methylergonovine maleate injection has been administered instead of vitamin k and hepatitis b vaccine, medications which are routinely administered to the newborn. due to the potential for accidental neonatal exposure, methylergonovine maleate injections should be stored separately from medications intended for neonatal administration.

Dosage and Administration:

Dosage & administration parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration. intramuscularly 1 ml, 0.2 mg, after delivery of the anterior shoulder, after delivery of the placenta, or during the puerperium. may be repeated as required, at intervals of 2-4 hours. intravenously 1 ml, 0.2 mg, administered slowly over a period of no less than 60 seconds. (see warnings.)

Contraindications:

Contraindications hypertension; toxemia; pregnancy; and hypersensitivity.

Adverse Reactions:

Adverse reactions the most common adverse reaction is hypertension associated in several cases with seizure and/or headache. hypotension has also been reported. abdominal pain (caused by uterine contractions), nausea and vomiting have occurred occasionally. rarely observed reactions have included: acute myocardial infarction, transient chest pains, vasoconstriction, vasospasm, coronary arterial spasm, bradycardia, tachycardia, dyspnea, hematuria, thrombophlebitis, water intoxication, hallucinations, leg cramps, dizziness, tinnitus, nasal congestion, diarrhea, diaphoresis, palpitation, rash and foul taste. there have been rare isolated reports of anaphylaxis, without a proven causal relationship to the drug product. postmarketing experience the following adverse drug reactions have been derived from post-marketing experience with methylergonovine maleate injection via spontaneous case reports. because these reactions are reported voluntarily from a population of uncertain size, it is no
t possible to reliably estimate their frequency, which is therefore categorized as not known. nervous system disorders cerebrovascular accident, paraesthesia cardiac disorders ventricular fibrillation, ventricular tachycardia, angina pectoris, atrioventricular block

Overdosage:

Overdosage symptoms of acute overdose may include: nausea, vomiting, oliguria, abdominal pain, numbness, tingling of the extremities, and rise in blood pressure, in severe cases followed by hypotension, respiratory depression, hypothermia, convulsions, and coma. because reports of overdosage with methylergonovine maleate are infrequent, the lethal dose in humans has not been established. the oral ld50 (in mg/kg) for the mouse is 187, the rat 93, and the rabbit 4.5. several cases of accidental methylergonovine maleate injection in newborn infants have been reported, and in such cases 0.2 mg represents an overdose of great magnitude. however, recovery occurred in all but one case following a period of respiratory depression, hypothermia, hypertonicity with jerking movements, and convulsions. also, several children 1-3 years of age have accidentally ingested up to 10 tablets (2 mg) with no apparent ill effects. a postpartum patient took 4 tablets at one time in error and reported paraesthesias and clamminess as her only symptoms. treatment of acute overdosage is symptomatic and includes the usual procedures of: 1. removal of offending drug by inducing emesis, gastric lavage, catharsis, and supportive diuresis. 2. maintenance of adequate pulmonary ventilation, especially if convulsions or coma develop. 3. correction of hypotension with pressor drugs as needed. 4. control of convulsions with standard anticonvulsant agents. 5. control of peripheral vasospasm with warmth to the extremities if needed.

Description:

Description methylergonovine maleate injection, usp is a semi-synthetic ergot alkaloid used for the prevention and control of postpartum hemorrhage. methylergonovine maleate injection, usp is available in sterile ampules of 1 ml, containing 0.2 mg methylergonovine maleate for intramuscular or intravenous injection. ampules, 1 ml, clear, colorless solution. active ingredients: methylergonovine maleate, usp, 0.2 mg. inactive ingredients: maleic acid, 0.10 mg; sodium chloride, 7.0 mg; water for injection, qs to 1 ml. chemically, methylergonovine maleate is designated as ergoline-8-carboxamide, 9,10-didehydro-n-[l-(hydroxymethyl)propyl ]-6-methyl-, [8β(s)]-, (z)-2-butenedioate (1:1) (salt). its structural formula is: c20h25n3o2∙c4h4o4 mol. wt. - 455.51 description

Clinical Pharmacology:

Clinical pharmacology methylergonovine maleate acts directly on the smooth muscle of the uterus and increases the tone, rate, and amplitude of rhythmic contractions. thus, it induces a rapid and sustained tetanic uterotonic effect which shortens the third stage of labor and reduces blood loss. the onset of action after i.v. administration is immediate; after i.m. administration, 2-5 minutes, and after oral administration, 5-10 minutes. pharmacokinetic studies following an i.v. injection have shown that methylergonovine is rapidly distributed from plasma to peripheral tissues within 2-3 minutes or less. the bioavailability after oral administration was reported to be about 60%, with no accumulation after repeated doses. during delivery with intramuscular injection, bioavailability increased to 78%. ergot alkaloids are mostly eliminated by hepatic metabolism and excretion, and the decrease in bioavailability following oral administration is probably a result of first-pass metabolism in t
he liver. bioavailability studies conducted in fasting healthy female volunteers have shown that oral absorption of a 0.2 mg methylergonovine tablet was fairly rapid, with a mean peak plasma concentration of 3243 ± 1308 pg/ml observed at 1.12 ± 0.82 hours. for a 0.2 mg intramuscular injection, a mean peak plasma concentration of 5918 ± 1952 pg/ml was observed at 0.41 ± 0.21 hours. the extent of absorption of the tablet, based upon methylergonovine plasma concentrations, was found to be equivalent to that of the i.m. solution given orally, and the extent of oral absorption of the i.m. solution was proportional to the dose following administration of 0.1, 0.2, and 0.4 mg. when given intramuscularly, the extent of absorption of methylergonovine maleate solution was about 25% greater than the tablet. the volume of distribution (vdss/f) of methylergonovine was calculated to be 56.1 ± 17.0 liters, and the plasma clearance (clp/f) was calculated to be 14.4 ± 4.5 liters per hour. the plasma level decline was biphasic, with a mean elimination half-life of 3.39 hours (range 1.5 to 12.7 hours). a delayed gastrointestinal absorption (tmax about 3 hours) of methylergonovine maleate tablet might be observed in postpartum women during continuous treatment with this oxytocic agent.

How Supplied:

How supplied ampules store and dispense ampules store in refrigerator, 2°c-8°c (36°f-46°f). protect from light. administer only if solution is clear and colorless. hs

Package Label Principal Display Panel:

Principal display panel - 51662-1556-1, serialized vial serialized label

Principal display panel - ampule label ampule label


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