NDC 62756-139 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug 2 recalls

Product NDC62756-139

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077242
Marketed since
February 1, 2022
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
62756-139-0150 CAPSULE in 1 BOX, UNIT-DOSE (62756-139-01)Feb 1, 2022
62756-139-03100 CAPSULE in 1 BOTTLE (62756-139-03)Feb 1, 2022

Recalls mentioning this NDC

Other Gabapentin products