NDC 55154-7993 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug 2 recalls

Product NDC55154-7993

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Cardinal Health 107, LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA090858
Marketed since
January 29, 2011
Marketing end
August 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
55154-7993-010 BLISTER PACK in 1 BAG (55154-7993-0) / 1 CAPSULE in 1 BLISTER PACKJan 29, 2011

Recalls mentioning this NDC

Other Gabapentin products