65841-028 NDC - METFORMIN HYDROCHLORIDE ()

Drug Information

Product NDC: 65841-028

Proprietary Name: METFORMIN HYDROCHLORIDE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Pharmacy Class(es):
  • Biguanide [EPC];
  • Biguanides [CS]

Labeler Information

Labeler Name: Cadila Healthcare Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/20/2010

Package Information

No. Package Code Package Description Billing Unit
165841-028-01100 TABLET, FILM COATED in 1 BOTTLE (65841-028-01)
265841-028-05500 TABLET, FILM COATED in 1 BOTTLE (65841-028-05)
365841-028-101000 TABLET, FILM COATED in 1 BOTTLE (65841-028-10)
465841-028-1690 TABLET, FILM COATED in 1 BOTTLE (65841-028-16)
565841-028-6110 BAG in 1 DRUM (65841-028-61) / 1000 TABLET, FILM COATED in 1 BAG
665841-028-77100 BLISTER PACK in 1 CARTON (65841-028-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (65841-028-30)

NDC Record

Field Name Field Value Definition
PRODUCT NDC65841-028The 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 DATE3/20/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECadila Healthcare LimitedName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC65841-028The 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 DATE9/28/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEZydus Lifesciences LimitedName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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