NDC 43598-294 – Pregabalin

Pregabalin 100 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV 1 recall

Product NDC43598-294

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
43598-294-05500 CAPSULE in 1 BOTTLE (43598-294-05)Jul 19, 2019
43598-294-665 BLISTER PACK in 1 CARTON (43598-294-66) / 10 CAPSULE in 1 BLISTER PACK (43598-294-79)Jul 19, 2019
43598-294-7810 BLISTER PACK in 1 CARTON (43598-294-78) / 10 CAPSULE in 1 BLISTER PACK (43598-294-79)Jul 19, 2019
43598-294-9090 CAPSULE in 1 BOTTLE (43598-294-90)Jul 19, 2019

Recalls mentioning this NDC

Other Pregabalin products