67046-463 NDC - METFORMIN HYDROCHLORIDE ()

Drug Information

Product NDC: 67046-463

Proprietary Name: Metformin hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Contract Pharmacy Services-PA
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/20/2017

Package Information

No. Package Code Package Description Billing Unit
167046-463-077 TABLET in 1 BLISTER PACK (67046-463-07)
267046-463-1414 TABLET in 1 BLISTER PACK (67046-463-14)
367046-463-1515 TABLET in 1 BLISTER PACK (67046-463-15)
467046-463-2020 TABLET in 1 BLISTER PACK (67046-463-20)
567046-463-2121 TABLET in 1 BLISTER PACK (67046-463-21)
667046-463-2828 TABLET in 1 BLISTER PACK (67046-463-28)
767046-463-3030 TABLET in 1 BLISTER PACK (67046-463-30)
867046-463-6060 TABLET in 1 BLISTER PACK (67046-463-60)

NDC Record

Field Name Field Value Definition
PRODUCT NDC67046-463The 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 NAMEMetformin hydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/20/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEContract Pharmacy Services-PAName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023