Search Icon

0440-5746 NDC - METFORMIN HYDROCHLORIDE ()

Drug Information

Product NDC: 0440-5746

Proprietary Name: Metformin Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Liberty Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/31/2016

Package Information

No. Package Code Package Description Billing Unit
10440-5746-001000 TABLET, FILM COATED in 1 BOTTLE (0440-5746-00)EA
20440-5746-01100 TABLET, FILM COATED in 1 BOTTLE (0440-5746-01)EA
30440-5746-05500 TABLET, FILM COATED in 1 BOTTLE (0440-5746-05)EA
40440-5746-81300 TABLET, FILM COATED in 1 BOTTLE (0440-5746-81)EA
50440-5746-85800 TABLET, FILM COATED in 1 BOTTLE (0440-5746-85)EA
60440-5746-9090 TABLET, FILM COATED in 1 BOTTLE (0440-5746-90)EA
70440-5746-92180 TABLET, FILM COATED in 1 BOTTLE (0440-5746-92)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC0440-5746The 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 DATE3/31/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELiberty Pharmaceuticals, Inc.Name 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: 11/10/2022