NDC 68788-8790 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8790

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
December 16, 2024
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8790-1100 TABLET in 1 BOTTLE (68788-8790-1)Dec 16, 2024
68788-8790-330 TABLET in 1 BOTTLE (68788-8790-3)Dec 16, 2024
68788-8790-660 TABLET in 1 BOTTLE (68788-8790-6)Dec 16, 2024
68788-8790-8120 TABLET in 1 BOTTLE (68788-8790-8)Dec 16, 2024
68788-8790-990 TABLET in 1 BOTTLE (68788-8790-9)Dec 16, 2024

Other Gabapentin products