NDC 50090-6854 – Gabapentin

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

Human Prescription Drug

Product NDC50090-6854

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200651
Marketed since
October 6, 2011
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (3)

Package NDCDescriptionSince
50090-6854-090 TABLET, FILM COATED in 1 BOTTLE (50090-6854-0)Nov 30, 2023
50090-6854-160 TABLET, FILM COATED in 1 BOTTLE (50090-6854-1)Nov 30, 2023
50090-6854-230 TABLET, FILM COATED in 1 BOTTLE (50090-6854-2)Nov 30, 2023

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