NDC 42385-980 – Gabapentin

Gabapentin 800 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC42385-980

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Laurus Labs Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217965
Marketed since
April 9, 2024
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (6)

Package NDCDescriptionSince
42385-980-01100 TABLET, FILM COATED in 1 BOTTLE (42385-980-01)Apr 9, 2024
42385-980-05500 TABLET, FILM COATED in 1 BOTTLE (42385-980-05)Apr 9, 2024
42385-980-111000 TABLET, FILM COATED in 1 BOTTLE (42385-980-11)Apr 9, 2024
42385-980-3030 TABLET, FILM COATED in 1 BOTTLE (42385-980-30)Apr 9, 2024
42385-980-7210 BLISTER PACK in 1 CARTON (42385-980-72) / 10 TABLET, FILM COATED in 1 BLISTER PACKApr 9, 2024
42385-980-9090 TABLET, FILM COATED in 1 BOTTLE (42385-980-90)Apr 9, 2024

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