NDC 68071-2206 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-2206

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
February 4, 2016
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
68071-2206-1100 TABLET in 1 BOTTLE (68071-2206-1)Jul 6, 2020

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