NDC 69238-1316 – Pregabalin

Pregabalin 225 mg/1 · Capsule · Oral

Human Prescription Drug DEA schedule CV

Product NDC69238-1316

Product details

Brand name
Pregabalin
Generic name
Pregabalin
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA209743
Marketed since
July 19, 2019
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Pregabalin →

Package NDC codes (2)

Package NDCDescriptionSince
69238-1316-5500 CAPSULE in 1 BOTTLE (69238-1316-5)Jul 19, 2019
69238-1316-990 CAPSULE in 1 BOTTLE (69238-1316-9)Jul 19, 2019

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