NDC 70010-228 – Gabapentin

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

Human Prescription Drug 1 recall

Product NDC70010-228

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Granules Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217116
Marketed since
June 27, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
70010-228-01100 TABLET, FILM COATED in 1 BOTTLE (70010-228-01)Jun 27, 2023
70010-228-05500 TABLET, FILM COATED in 1 BOTTLE (70010-228-05)Jun 27, 2023

Recalls mentioning this NDC

Other Gabapentin products