Nystatin


Vistapharm, Inc.
Human Prescription Drug
NDC 66689-037
Nystatin is a human prescription drug labeled by 'Vistapharm, Inc.'. National Drug Code (NDC) number for Nystatin is 66689-037. This drug is available in dosage form of Suspension. The names of the active, medicinal ingredients in Nystatin drug includes Nystatin - 100000 [USP'U]/mL . The currest status of Nystatin drug is Active.

Drug Information:

Drug NDC: 66689-037
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: Nystatin
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: Nystatin
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Vistapharm, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Suspension
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:NYSTATIN - 100000 [USP'U]/mL
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: 10 May, 2010
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 29 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: ANDA064142
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:VistaPharm, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:312055
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.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
NUI:N0000175498
M0017172
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:BDF1O1C72E
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 EPC:Polyene Antifungal [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class CS:Polyenes [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Polyene Antifungal [EPC]
Polyenes [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
66689-037-505 TRAY in 1 CASE (66689-037-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (66689-037-01)10 May, 2010N/ANo
66689-037-9910 TRAY in 1 CASE (66689-037-99) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (66689-037-01)10 May, 2010N/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:

Nystatin nystatin nystatin nystatin methylparaben sodium phosphate, dibasic, anhydrous sodium phosphate, monobasic, monohydrate glycerin saccharin sodium sucrose carboxymethylcellulose sodium alcohol propylparaben light yellow nystatin nystatin nystatin nystatin alcohol carboxymethylcellulose sodium sodium phosphate, dibasic glycerin methylparaben sodium phosphate, monobasic propylparaben water saccharin sodium sucrose light yellow

Indications and Usage:

Indications and usage nystatin oral suspension, usp, is indicated for the treatment of candidiasis in the oral cavity.

General Precautions:

General this medication is not to be used for the treatment of systemic mycoses. discontinue treatment if sensitization or irritation is reported during use.

Dosage and Administration:

Dosage and administration infants: 2 ml (200,000 units) four times daily (in infants and young children, use dropper to place one-half of dose in each side of mouth and avoid feeding for 5 to 10 minutes). note: limited clinical studies in premature and low birth weight infants indicate that 1 ml four times daily is effective. children and adults: 4 to 6 ml (400,000 to 600,000 units) four times daily (one-half of dose in each side of mouth). the preparation should be retained in the mouth as long as possible before swallowing. continue treatment for at least 48 hours after perioral symptoms have disappeared and cultures demonstrate eradication of candida albicans .

Contraindications:

Contraindications the preparation is contraindicated in patients with a history of hypersensitivity to any of its components.

Adverse Reactions:

Adverse reactions nystatin is well tolerated even with prolonged therapy. oral irritation and sensitization have been reported. (see precautions: general ). gastrointestinal : diarrhea (including one case of bloody diarrhea), nausea, vomiting, gastrointestinal upset/disturbances. dermatologic : rash, including urticaria has been reported rarely. stevens-johnson syndrome has been reported very rarely. other : tachycardia, bronchospasm, facial swelling, and nonspecific myalgia have also been rarely reported. to report suspected adverse reactions, contact vistapharm, inc., at 1-888-655-1505 or fda at 1-800-fda-1088 or www.fda.gov/medwatch.

Use in Pregnancy:

Pregnancy: teratogenic effects category c animal reproduction studies have not been conducted with nystatin oral suspension. it is also not known whether nystatin oral suspension can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. nystatin oral suspension should be given to a pregnant woman only if clearly needed.

Pediatric Use:

Pediatric use see dosage and administration .

Overdosage:

Overdosage oral doses of nystatin in excess of five million units daily have caused nausea and gastrointestinal upset. there have been no reports of serious toxic effects of superinfections (see clinical pharmacology: pharmacokinetics ).

Description:

Description nystatin is an antimycotic polyene antibiotic obtained from streptomyces noursei . structural formula: nystatin oral suspension, usp, for oral administration, contains 100,000 nystatin units per ml. inactive ingredients (cherry flavor): alcohol (­ 1% v/v), methylparaben, nf; dibasic sodium phosphate, usp; monobasic sodium phosphate, usp; saccharin sodium, usp; sucrose (50% w/v), nf; glycerin, usp; carboxy-methylcellulose sodium, usp; propylparaben, nf; artificial wild cherry flavor # 14783 and purified water, usp. inactive ingredients (bubblegum flavor): alcohol (0.5% v/v), usp, alcohol free bubblegum flavoring, carboxymethylcellulose sodium, usp, dibasic sodium phosphate, usp, glycerin natural 99.5%, usp, methylparaben, nf, (preservative), monobasic sodium phosphate, usp, propylparaben, nf, (preservative), purified water, usp, saccharin sodium, usp, and sucrose, nf. nystatin structure

Clinical Pharmacology:

Clinical pharmacology pharmacokinetics gastrointestinal absorption of nystatin is insignificant. most orally administered nystatin is passed unchanged in the stool. in patients with renal insufficiency receiving oral therapy with conventional dosage forms, significant plasma concentrations of nystatin may occasionally occur. microbiology nystatin is both fungistatic and fungicidal in vitro against a wide variety of yeasts and yeast-like fungi. candida albicans demonstrates no significant resistance to nystatin in vitro on repeated subculture in increasing levels of nystatin; other candida species become quite resistant. generally, resistance does not develop in vivo . nystatin acts by binding to sterols in the cell membrane of susceptible candida species with a resultant change in membrane permeability allowing leakage of intracellular components. nystatin exhibits no appreciable activity against bacteria, protozoa, or viruses.

Pharmacodynamics:

Pharmacokinetics gastrointestinal absorption of nystatin is insignificant. most orally administered nystatin is passed unchanged in the stool. in patients with renal insufficiency receiving oral therapy with conventional dosage forms, significant plasma concentrations of nystatin may occasionally occur.

Pharmacokinetics:

Microbiology nystatin is both fungistatic and fungicidal in vitro against a wide variety of yeasts and yeast-like fungi. candida albicans demonstrates no significant resistance to nystatin in vitro on repeated subculture in increasing levels of nystatin; other candida species become quite resistant. generally, resistance does not develop in vivo . nystatin acts by binding to sterols in the cell membrane of susceptible candida species with a resultant change in membrane permeability allowing leakage of intracellular components. nystatin exhibits no appreciable activity against bacteria, protozoa, or viruses.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility no long-term animal studies have been performed to evaluate carcinogenic potential. there also have been no studies to determine mutagenicity or whether this medication affects fertility in males or females.

How Supplied:

How supplied nystatin oral suspension, usp, 100,000 nystatin units per ml, cherry flavored, light creamy yellow, ready-to-use suspension, is available as follows: ndc 66689-037-01: 5 ml unit dose cup. ndc 66689-037-50: case contains 50 unit dose cups of 5 ml (ndc 66689-037-01), packaged in 5 trays of 10 unit dose cups each. ndc 66689-037-99: case contains 100 unit dose cups of 5 ml (ndc 66689-037-01), packaged in 10 trays of 10 unit dose cups each. nystatin oral suspension, usp, 100,000 nystatin units per ml, bubblegum flavored, yellow opaque, ready-to-use suspension is available as follows: ndc 66689-008-02: 2 fl. oz. bottle (60 ml): supplied in individual carton with calibrated dropper. ndc 66689-008-08: 8 fl. oz. bottle (237 ml). ndc 66689-008-16: 16 fl. oz. bottle (480 ml).

Package Label Principal Display Panel:

Principal display panel - unit dose cup nystatin oral suspension, usp 500,000 units/5 ml alcohol not more than 1% v/v shake well. avoid freezing. delivers 5 ml store at 20°–25°c (68°–77°f); see usp crt conditions. manufactured by: largo, fl 33771, usa xact dose™ vistapharm rx only vp2052r2 06/18 ndc 66689-037-01 lidding

Principal display panel - 60 ml ndc 66689-008-02 nystatin oral suspension, usp 100,000 units per ml contains: alcohol 0.5% v/v (bubblegum flavored) shake well before using at the time of dispensing replace cap with safety cap dropper 2 fl. oz. (60 ml) rx only vistapharm® ndc 66689-008-02 nystatin oral suspension, usp 100,000 units per ml contains: alcohol 0.5% v/v (bubblegum flavored) shake well before using 2 fl. oz. (60 ml) rx only vistapharm® 60 ml bottle 60 ml carton

Principal display panel - 480 ml ndc 66689-008-16 nystatin oral suspension, usp 100,000 units per ml contains: alcohol 0.5% v/v (bubblegum flavored) shake well before using 16 fl. oz. (480 ml) rx only vistapharm® ndc 66689-008-16 nystatin oral suspension, usp 100,000 units per ml (bubblegum flavored) contains: alcohol 0.5% v/v shake well before using 16 fl. oz. (480 ml) rx only vistapharm® 480 ml bottle 480 ml carton


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