72934-5143 NDC - METRONIDAZOLE 1% / MUPIROCIN 2% ()

Drug Information

  • Product NDC: 72934-5143
  • Proprietary Name: METRONIDAZOLE 1% / MUPIROCIN 2%
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Sincerus Florida, LLC
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:5/15/2019

Package Information

No. Package Code Package Description Billing Unit
172934-5143-230 g in 1 BOTTLE, PUMP (72934-5143-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72934-5143The 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 NAMEMETRONIDAZOLE 1% / MUPIROCIN 2%The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/15/2019The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERThe translation of the dosage form Code submitted by the firm.
LABELER NAMESincerus Florida, LLCThe translation of the route code submitted by the firm, indicating route of administration.

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This page was last updated on: 4/14/2026

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