NDC 72189-313 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-313

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Directrx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
January 17, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
72189-313-6060 TABLET in 1 BOTTLE (72189-313-60)Jan 17, 2022
72189-313-72120 TABLET in 1 BOTTLE (72189-313-72)Jan 17, 2022
72189-313-9090 TABLET in 1 BOTTLE (72189-313-90)Jan 17, 2022

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