NDC 72888-051 – Pregabalin

Pregabalin 330 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug DEA schedule CV

Product NDC72888-051

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Advagen Pharma Ltd.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215249
Marketed since
March 22, 2022
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (1)

Package NDCDescriptionSince
72888-051-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-051-30)Mar 22, 2022

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