NDC 80425-0201 – Gabapentin

Gabapentin 600 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC80425-0201

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA207057
Marketed since
October 28, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (4)

Package NDCDescriptionSince
80425-0201-130 TABLET, COATED in 1 BOTTLE (80425-0201-1)Oct 28, 2022
80425-0201-260 TABLET, COATED in 1 BOTTLE (80425-0201-2)Oct 28, 2022
80425-0201-390 TABLET, COATED in 1 BOTTLE (80425-0201-3)Oct 28, 2022
80425-0201-4120 TABLET, COATED in 1 BOTTLE (80425-0201-4)Oct 28, 2022

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