0187-5202 NDC - NORITATE (METRONIDAZOLE)

Drug Information

Product NDC: 0187-5202

Proprietary Name: Noritate

Non Proprietary Name: metronidazole

Active Ingredient(s):
  • 10 mg/60g METRONIDAZOLE


Administration Route(s): TOPICAL

Dosage Form(s): CREAM

Pharmacy Class(es):
  • Nitroimidazole Antimicrobial [EPC];
  • Nitroimidazoles [CS]

Labeler Information

Labeler Name: Bausch Health US, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020743
Marketing Category: NDA
Start Marketing Date:8/9/2013

Package Information

No. Package Code Package Description Billing Unit
10187-5202-353.5 g in 1 TUBE (0187-5202-35)
20187-5202-6060 g in 1 TUBE (0187-5202-60)GM

NDC Record

Field Name Field Value Definition
PRODUCT NDC0187-5202The 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 NAMENoritateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEmetronidazoleThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECREAMThe 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 DATE8/9/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAProduct 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 NUMBERNDA020743This 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 NAMEBausch Health US, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEMETRONIDAZOLEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH10 
ACTIVE INGRED UNITmg/60g 
PHARM CLASSESNitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS] 

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This page was last updated on: 10/4/2019