NDC 68788-8472 – Pregabalin

Pregabalin 50 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC68788-8472

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA206912
Marketed since
June 29, 2023
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8472-1100 CAPSULE in 1 BOTTLE (68788-8472-1)Jun 29, 2023
68788-8472-330 CAPSULE in 1 BOTTLE (68788-8472-3)Jun 29, 2023
68788-8472-660 CAPSULE in 1 BOTTLE (68788-8472-6)Jun 29, 2023
68788-8472-990 CAPSULE in 1 BOTTLE (68788-8472-9)Jun 29, 2023

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