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0472-0155 NDC - NYSTATIN AND TRIAMCINOLONE ACETONIDE

Drug Information

Product NDC: 0472-0155

Proprietary Name: Nystatin and Triamcinolone Acetonide

Non Proprietary Name: Nystatin and Triamcinolone Acetonide

Active Ingredient(s):
  • 100000 [USP'U]/g NYSTATIN;
  • 1 mg/g TRIAMCINOLONE ACETONIDE


Administration Route(s): TOPICAL

Dosage Form(s): OINTMENT

Pharmacy Class(es):
  • Corticosteroid Hormone Receptor Agonists [MoA];
  • Corticosteroid [EPC];
  • Polyene Antifungal [EPC];
  • Polyenes [CS]

Labeler Information

Labeler Name: Actavis Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062733
Marketing Category: ANDA
Start Marketing Date:6/5/2015
End Marketing Date:3/31/2023

Package Information

No. Package Code Package Description Billing Unit
10472-0155-151 TUBE in 1 CARTON (0472-0155-15) > 15 g in 1 TUBE
20472-0155-301 TUBE in 1 CARTON (0472-0155-30) > 30 g in 1 TUBE
30472-0155-601 TUBE in 1 CARTON (0472-0155-60) > 60 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC0472-0155The 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.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMENystatin and Triamcinolone AcetonideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMENystatin and Triamcinolone AcetonideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEOINTMENTThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/5/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE3/31/2023This 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.
MARKETING CATEGORY NAMEANDAProduct types are broken down into several potential Marketing Categories, such as NDA/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.
APPLICATION NUMBERANDA062733This 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.
LABELER NAMEActavis Pharma, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMENYSTATIN; TRIAMCINOLONE ACETONIDEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH100000; 1 
ACTIVE INGRED UNIT[USP'U]/g; mg/g 
PHARM CLASSESCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Polyene Antifungal [EPC], Polyenes [CS] 

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This page was last updated on: 10/28/2022