NDC 72189-158 – Gabapentin

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

Human Prescription Drug

Product NDC72189-158

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
DIRECT RX
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203244
Marketed since
December 1, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
72189-158-3030 TABLET, FILM COATED in 1 BOTTLE (72189-158-30)Dec 1, 2020
72189-158-6060 TABLET, FILM COATED in 1 BOTTLE (72189-158-60)Dec 1, 2020
72189-158-72120 TABLET, FILM COATED in 1 BOTTLE (72189-158-72)Dec 1, 2020
72189-158-9090 TABLET, FILM COATED in 1 BOTTLE (72189-158-90)Dec 1, 2020

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