NDC 76420-235 – Gabapentin

Gabapentin 600 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76420-235

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Asclemed USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
February 4, 2016
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (5)

Package NDCDescriptionSince
76420-235-12120 TABLET in 1 BOTTLE (76420-235-12)Jul 7, 2022
76420-235-24240 TABLET in 1 BOTTLE (76420-235-24)Jul 7, 2022
76420-235-3030 TABLET in 1 BOTTLE (76420-235-30)Jul 7, 2022
76420-235-6060 TABLET in 1 BOTTLE (76420-235-60)Jul 7, 2022
76420-235-9090 TABLET in 1 BOTTLE (76420-235-90)Jul 7, 2022

Other Gabapentin products