Metformin Hydrochloride 500 mg/1
Metformin Hydrochloride Extended-Release Tablets · TABLET, FILM COATED, EXTENDED RELEASE · AiPing Pharmaceutical, Inc.
Metformin Hydrochloride is a tablet, film coated, extended release containing metformin hydrochloride extended-release tablets at 500 mg/1, taken oral. Manufactured by AiPing Pharmaceutical, Inc..
Key Facts
- Brand Name
- Metformin Hydrochloride
- Generic Name
- Metformin Hydrochloride Extended-Release Tablets
- NDC Code (Product)
11788-037- Manufacturer
- AiPing Pharmaceutical, Inc.
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA209993
- Marketing Start
- 12/15/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is Metformin Hydrochloride used for?
Metformin Hydrochloride contains Metformin Hydrochloride Extended-Release Tablets. It is a tablet, film coated, extended release taken oral. Consult your doctor for specific uses.
Is Metformin Hydrochloride a controlled substance?
Metformin Hydrochloride is not classified as a controlled substance by the DEA.
What is the generic name for Metformin Hydrochloride?
The generic name for Metformin Hydrochloride is Metformin Hydrochloride Extended-Release Tablets. There are no other listed brand versions of Metformin Hydrochloride Extended-Release Tablets.
What is the NDC code for Metformin Hydrochloride 500 mg/1?
The NDC (National Drug Code) for Metformin Hydrochloride 500 mg/1 is 11788-037, listed by AiPing Pharmaceutical, Inc..
Product NDC
11788-037
Package NDC
- 11788-037-60
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (11788-037-60)
Other Metformin Hydrochloride Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)