NDC 67296-0700

Metformin Hydrochloride 1000 mg tablet, film coated

On the label: RedPharm Drug. Inc.. It's a repackaged product: RedPharm Drug. Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-010.

Where the pills inside were made

Aurobindo Pharma Limited

Medchal, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.

Aurobindo Pharma Limited

Mahabubnagar, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection May 10, 2022. 7 inspections on record, 1 with serious problems.

Repackaging site

Recalls

Product details

Generic drug
Metformin: see every company that makes it
Form
tablet, film coated
Strength
1000 mg
Approval
ANDA ANDA077095
On the market since
Jan 14, 2005
Package NDCs
67296-0700-1 67296-0700-3
Official label
DailyMed (National Library of Medicine), updated Jan 19, 2022

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