NDC 83301-0002 – Gabapentin

Gabapentin 800 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC83301-0002

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Mullan Pharmaceutical Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA207057
Marketed since
January 1, 2024
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
83301-0002-1100 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0002-1)Jan 1, 2024
83301-0002-2500 TABLET, COATED in 1 BOTTLE, PLASTIC (83301-0002-2)Jan 1, 2024

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