NDC 72189-471 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-471

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Direct_Rx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
May 15, 2023
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
72189-471-3030 TABLET in 1 BOTTLE (72189-471-30)May 15, 2023
72189-471-6060 TABLET in 1 BOTTLE (72189-471-60)May 15, 2023
72189-471-72120 TABLET in 1 BOTTLE (72189-471-72)May 15, 2023
72189-471-9090 TABLET in 1 BOTTLE (72189-471-90)May 15, 2023

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