NDC 80425-0158 – Gabapentin

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

Human Prescription Drug

Product NDC80425-0158

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200651
Marketed since
October 6, 2011
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
80425-0158-130 TABLET, FILM COATED in 1 BOTTLE (80425-0158-1)Oct 6, 2011
80425-0158-260 TABLET, FILM COATED in 1 BOTTLE (80425-0158-2)Oct 6, 2011

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