NDC 50228-462 – Pregabalin Extended Release

Pregabalin 82.5 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CV

Product NDC50228-462

Product details

Brand name
Pregabalin Extended Release
Generic name
Pregabalin
Labeler
ScieGen Pharmaceuticals, INC.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215675
Marketed since
September 14, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin Extended Release →

Package NDC codes (2)

Package NDCDescriptionSince
50228-462-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-462-05)Sep 14, 2022
50228-462-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50228-462-30)Sep 14, 2022

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