NDC 72205-077 – Pregabalin

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

Human Prescription Drug DEA schedule CV

Product NDC72205-077

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Novadoz Pharmaceuticals LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213226
Marketed since
April 13, 2021
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (1)

Package NDCDescriptionSince
72205-077-3030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72205-077-30)Apr 13, 2021

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