NDC 72189-394 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-394

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Direct_Rx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
November 16, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
72189-394-3030 TABLET in 1 BOTTLE (72189-394-30)Nov 16, 2022
72189-394-6060 TABLET in 1 BOTTLE (72189-394-60)Nov 16, 2022
72189-394-72120 TABLET in 1 BOTTLE (72189-394-72)Nov 16, 2022
72189-394-9090 TABLET in 1 BOTTLE (72189-394-90)Nov 16, 2022

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