NDC 68071-5310 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-5310

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206402
Marketed since
November 1, 2015
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
68071-5310-990 TABLET in 1 BOTTLE (68071-5310-9)Jul 22, 2026

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