NDC 69367-304 – Miglitol

Miglitol 50 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC69367-304

Product details

Brand name
Miglitol
Generic name
Miglitol
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA203965
Marketed since
January 15, 2021
Listing expires
December 31, 2026
Pharmacologic class
alpha-Glucosidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Miglitol →

Package NDC codes (1)

Package NDCDescriptionSince
69367-304-01100 TABLET, COATED in 1 BOTTLE (69367-304-01)Jan 15, 2021

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