NDC 68788-7757 – Gabapentin

Gabapentin 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7757

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205101
Marketed since
July 1, 2020
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (5)

Package NDCDescriptionSince
68788-7757-1100 TABLET in 1 BOTTLE (68788-7757-1)Jul 1, 2020
68788-7757-330 TABLET in 1 BOTTLE (68788-7757-3)Jul 1, 2020
68788-7757-660 TABLET in 1 BOTTLE (68788-7757-6)Jul 1, 2020
68788-7757-8120 TABLET in 1 BOTTLE (68788-7757-8)Jul 1, 2020
68788-7757-990 TABLET in 1 BOTTLE (68788-7757-9)Jul 1, 2020

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