Drugplain

Metformin Hydrochloride 850 mg/1

Metformin Hydrochloride · TABLET, FILM COATED · MARKSANS PHARMA LIMITED

No Recall History
Plain English

Metformin Hydrochloride is a tablet, film coated containing metformin hydrochloride at 850 mg/1, taken oral. Manufactured by MARKSANS PHARMA LIMITED.

Key Facts

Brand Name
Metformin Hydrochloride
Generic Name
Metformin Hydrochloride
NDC Code (Product)
25000-131
Manufacturer
MARKSANS PHARMA LIMITED
Strength
850 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA090888
Marketing Start
06/01/2012

Recall History

No Recall History

Frequently Asked Questions

What is Metformin Hydrochloride used for?

Metformin Hydrochloride contains Metformin Hydrochloride. It is a tablet, film coated 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. There are 5 other brand versions of Metformin Hydrochloride.

What is the NDC code for Metformin Hydrochloride 850 mg/1?

The NDC (National Drug Code) for Metformin Hydrochloride 850 mg/1 is 25000-131, listed by MARKSANS PHARMA LIMITED.

Product NDC

25000-131

Package NDCs (3)

  • 25000-131-03

    30 TABLET, FILM COATED in 1 BOTTLE (25000-131-03)

  • 25000-131-12

    500 TABLET, FILM COATED in 1 BOTTLE (25000-131-12)

  • 25000-131-52

    1800 TABLET, FILM COATED in 1 BAG (25000-131-52)

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)