NDC 43598-296 – pregabalin

Pregabalin 200 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV 1 recall

Product NDC43598-296

Product details

Brand name
pregabalin
Generic name
pregabalin
Labeler
Dr.Reddys Laboratories Inc
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA209664
Marketed since
July 19, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (4)

Package NDCDescriptionSince
43598-296-05500 CAPSULE in 1 BOTTLE (43598-296-05)Jul 19, 2019
43598-296-665 BLISTER PACK in 1 CARTON (43598-296-66) / 10 CAPSULE in 1 BLISTER PACK (43598-296-79)Jul 19, 2019
43598-296-7810 BLISTER PACK in 1 CARTON (43598-296-78) / 10 CAPSULE in 1 BLISTER PACK (43598-296-79)Jul 19, 2019
43598-296-9090 CAPSULE in 1 BOTTLE (43598-296-90)Jul 19, 2019

Recalls mentioning this NDC

Other Pregabalin products