Drugplain

Metformin Hydrochloride 1000 mg/1

Metformin Hydrochloride Extended-Release Tablets · TABLET, FILM COATED, EXTENDED RELEASE · ScieGen Pharmaceuticals, Inc.

No Recall History
Plain English

Metformin Hydrochloride is a tablet, film coated, extended release containing metformin hydrochloride extended-release tablets at 1000 mg/1, taken oral. Manufactured by ScieGen Pharmaceuticals, Inc..

Key Facts

Brand Name
Metformin Hydrochloride
Generic Name
Metformin Hydrochloride Extended-Release Tablets
NDC Code (Product)
50228-504
Manufacturer
ScieGen Pharmaceuticals, Inc.
Strength
1000 mg/1
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA214629
Marketing Start
02/22/2022

Recall History

No Recall History

Frequently 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 1000 mg/1?

The NDC (National Drug Code) for Metformin Hydrochloride 1000 mg/1 is 50228-504, listed by ScieGen Pharmaceuticals, Inc..

Product NDC

50228-504

Package NDCs (3)

  • 50228-504-05

    500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-504-05)

  • 50228-504-30

    30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-504-30)

  • 50228-504-60

    60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-504-60)

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

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