NDC 72578-036 – Metformin Hydrochloride

Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 2 recalls

Product NDC72578-036

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Viona Pharmaceuticals Inc
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077078
Marketed since
March 15, 2019
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

Uses, dosage, side effects and warnings for Metformin hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
72578-036-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-01)Mar 15, 2019
72578-036-05500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-05)Mar 15, 2019

Recalls mentioning this NDC

Other Metformin hydrochloride products