NDC 70518-2912 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-2912

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206402
Marketed since
October 20, 2020
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
70518-2912-2100 POUCH in 1 BOX (70518-2912-2) / 1 TABLET in 1 POUCH (70518-2912-3)Mar 19, 2023

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