NDC 12634-172 Metronidazole

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
12634-172
Proprietary Name:
Metronidazole
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apotheca Inc.
Labeler Code:
12634
Start Marketing Date: [9]
06-01-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
18 MM
Imprint(s):
U;227
Score:
1

Product Packages

NDC Code 12634-172-00

Package Description: 10 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-01

Package Description: 100 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-48

Package Description: 21 TABLET, FILM COATED in 1 BLISTER PACK

NDC Code 12634-172-50

Package Description: 50 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-71

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-78

Package Description: 28 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-79

Package Description: 25 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-80

Package Description: 20 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-81

Package Description: 21 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-84

Package Description: 14 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-94

Package Description: 4 TABLET, FILM COATED in 1 BOTTLE

NDC Code 12634-172-99

Package Description: 9 TABLET, FILM COATED in 1 BOTTLE

Product Details

What is NDC 12634-172?

The NDC code 12634-172 is assigned by the FDA to the product Metronidazole which is product labeled by Apotheca Inc.. The product's dosage form is . The product is distributed in 12 packages with assigned NDC codes 12634-172-00 10 tablet, film coated in 1 bottle , 12634-172-01 100 tablet, film coated in 1 bottle , 12634-172-48 21 tablet, film coated in 1 blister pack , 12634-172-50 50 tablet, film coated in 1 bottle , 12634-172-71 30 tablet, film coated in 1 bottle , 12634-172-78 28 tablet, film coated in 1 bottle , 12634-172-79 25 tablet, film coated in 1 bottle , 12634-172-80 20 tablet, film coated in 1 bottle , 12634-172-81 21 tablet, film coated in 1 bottle , 12634-172-84 14 tablet, film coated in 1 bottle , 12634-172-94 4 tablet, film coated in 1 bottle , 12634-172-99 9 tablet, film coated in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Metronidazole?

Metronidazole is an antibiotic that is used to treat a wide variety of infections. It works by stopping the growth of certain bacteria and parasites. This antibiotic treats only certain bacterial and parasitic infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections. Metronidazole may also be used with other medications to treat certain stomach/intestinal ulcers caused by a bacteria (H. pylori).

Which are Metronidazole UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Metronidazole Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Metronidazole?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".