71335-0858 NDC - METRONIDAZOLE ()

Drug Information

Product NDC: 71335-0858

Proprietary Name: Metronidazole

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Bryant Ranch Prepack
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/30/1990

Package Information

No. Package Code Package Description Billing Unit
171335-0858-07 TABLET in 1 BOTTLE (71335-0858-0)
271335-0858-121 TABLET in 1 BOTTLE (71335-0858-1)
371335-0858-230 TABLET in 1 BOTTLE (71335-0858-2)
471335-0858-320 TABLET in 1 BOTTLE (71335-0858-3)
571335-0858-460 TABLET in 1 BOTTLE (71335-0858-4)
671335-0858-528 TABLET in 1 BOTTLE (71335-0858-5)
771335-0858-614 TABLET in 1 BOTTLE (71335-0858-6)
871335-0858-740 TABLET in 1 BOTTLE (71335-0858-7)
971335-0858-842 TABLET in 1 BOTTLE (71335-0858-8)
1071335-0858-956 TABLET in 1 BOTTLE (71335-0858-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71335-0858The 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 NAMEMetronidazoleThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/30/1990This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBryant Ranch PrepackName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024