NDC 72189-619 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-619

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Direct_Rx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206402
Marketed since
March 18, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
72189-619-72120 TABLET in 1 BOTTLE (72189-619-72)Mar 18, 2025
72189-619-9090 TABLET in 1 BOTTLE (72189-619-90)Mar 18, 2025

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