NDC 70518-2356 – Gabapentin

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

Human Prescription Drug

Product NDC70518-2356

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200651
Marketed since
October 9, 2019
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (2)

Package NDCDescriptionSince
70518-2356-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-2356-0)Oct 9, 2019
70518-2356-190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2356-1)Oct 21, 2019

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