NDC 68788-8468 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8468

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214957
Marketed since
June 26, 2023
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8468-1100 TABLET in 1 BOTTLE (68788-8468-1)Jun 26, 2023
68788-8468-330 TABLET in 1 BOTTLE (68788-8468-3)Jun 26, 2023
68788-8468-660 TABLET in 1 BOTTLE (68788-8468-6)Jun 26, 2023
68788-8468-8120 TABLET in 1 BOTTLE (68788-8468-8)Jun 26, 2023
68788-8468-990 TABLET in 1 BOTTLE (68788-8468-9)Jun 26, 2023

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