NDC 72162-2141 – Gabapentin

Gabapentin 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72162-2141

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203244
Marketed since
January 11, 2014
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
72162-2141-1100 TABLET, FILM COATED in 1 BOTTLE (72162-2141-1)Oct 12, 2023
72162-2141-5500 TABLET, FILM COATED in 1 BOTTLE (72162-2141-5)Oct 12, 2023

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