NDC 70518-2098 – Gabapentin

Gabapentin 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-2098

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203244
Marketed since
May 22, 2019
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (1)

Package NDCDescriptionSince
70518-2098-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-2098-0)May 22, 2019

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