NDC 45963-556 – Gabapentin

Gabapentin 300 mg/1 · Capsule · Oral

Human Prescription Drug 3 recalls

Product NDC45963-556

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Actavis Pharma, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA075350
Marketed since
April 3, 2014
Marketing end
May 31, 2028

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
45963-556-11100 CAPSULE in 1 BOTTLE (45963-556-11)Apr 3, 2014
45963-556-50500 CAPSULE in 1 BOTTLE (45963-556-50)May 12, 2014

Recalls mentioning this NDC

Other Gabapentin products