NDC 68788-7774 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7774

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
August 24, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (5)

Package NDCDescriptionSince
68788-7774-1100 TABLET in 1 BOTTLE (68788-7774-1)Aug 24, 2020
68788-7774-330 TABLET in 1 BOTTLE (68788-7774-3)Aug 24, 2020
68788-7774-660 TABLET in 1 BOTTLE (68788-7774-6)Aug 24, 2020
68788-7774-8120 TABLET in 1 BOTTLE (68788-7774-8)Aug 24, 2020
68788-7774-990 TABLET in 1 BOTTLE (68788-7774-9)Aug 24, 2020

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