NDC 68788-7838 – Gabapentin

Gabapentin 400 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68788-7838

Product details

Brand name
Gabapentin
Generic name
Gabapentin
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204989
Marketed since
January 18, 2021
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Gabapentin →

Package NDC codes (5)

Package NDCDescriptionSince
68788-7838-1100 CAPSULE in 1 BOTTLE, PLASTIC (68788-7838-1)Jan 18, 2021
68788-7838-330 CAPSULE in 1 BOTTLE, PLASTIC (68788-7838-3)Jan 18, 2021
68788-7838-660 CAPSULE in 1 BOTTLE, PLASTIC (68788-7838-6)Jan 18, 2021
68788-7838-8120 CAPSULE in 1 BOTTLE, PLASTIC (68788-7838-8)Jan 18, 2021
68788-7838-990 CAPSULE in 1 BOTTLE, PLASTIC (68788-7838-9)Jan 18, 2021

Other Gabapentin products