NDC 68071-3523 – Gabapentin

Gabapentin 800 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68071-3523

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA207057
Marketed since
November 1, 2021
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
68071-3523-990 TABLET, COATED in 1 BOTTLE, PLASTIC (68071-3523-9)Oct 12, 2023

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