NDC 50090-6189 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-6189

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
October 1, 2021
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
50090-6189-060 TABLET in 1 BOTTLE (50090-6189-0)Oct 27, 2022
50090-6189-190 TABLET in 1 BOTTLE (50090-6189-1)Oct 27, 2022
50090-6189-230 TABLET in 1 BOTTLE (50090-6189-2)Oct 27, 2022

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