NDC 47335-687 – Pregabalin

Pregabalin 50 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV 1 recall

Product NDC47335-687

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA091157
Marketed since
December 4, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (4)

Package NDCDescriptionSince
47335-687-08100 CAPSULE in 1 BOTTLE (47335-687-08)Dec 4, 2019
47335-687-181000 CAPSULE in 1 BOTTLE (47335-687-18)Dec 4, 2019
47335-687-8330 CAPSULE in 1 BOTTLE (47335-687-83)Dec 4, 2019
47335-687-88100 CAPSULE in 1 BOTTLE (47335-687-88)Dec 4, 2019

Recalls mentioning this NDC

Other Pregabalin products