71717-106 NDC - METFORMIN HYDROCHLORIDE ()

Drug Information

Product NDC: 71717-106

Proprietary Name: METFORMIN HYDROCHLORIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Megalith Pharmaceuticals Inc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/18/2017

Package Information

No. Package Code Package Description Billing Unit
171717-106-111000 TABLET, COATED in 1 BOTTLE (71717-106-11)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC71717-106The 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 DATE12/18/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMegalith Pharmaceuticals IncName 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