NDC 76282-406 – Gabapentin

Gabapentin 800 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC76282-406

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Exelan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202764
Marketed since
November 2, 2012
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
76282-406-01100 TABLET, FILM COATED in 1 BOTTLE (76282-406-01)Nov 2, 2012
76282-406-05500 TABLET, FILM COATED in 1 BOTTLE (76282-406-05)Nov 2, 2012
76282-406-3030 TABLET, FILM COATED in 1 BOTTLE (76282-406-30)Nov 2, 2012
76282-406-9090 TABLET, FILM COATED in 1 BOTTLE (76282-406-90)Nov 2, 2012

Recalls mentioning this NDC

Other Gabapentin products