NDC 62756-137 – gabapentin

Gabapentin 100 mg/1 · Capsule · Oral

Human Prescription Drug 2 recalls

Product NDC62756-137

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
62756-137-0150 CAPSULE in 1 BOX, UNIT-DOSE (62756-137-01)Feb 1, 2022
62756-137-03100 CAPSULE in 1 BOTTLE (62756-137-03)Feb 1, 2022

Recalls mentioning this NDC

Other Gabapentin products