NDC 51224-121 – Gabapentin

Gabapentin 800 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC51224-121

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
TAGI Pharma, Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA207057
Marketed since
May 1, 2019
Marketing end
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
51224-121-60500 TABLET, COATED in 1 BOTTLE (51224-121-60)May 1, 2019

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