FDA NDC Directory · JSON-LD · Markdown

Pregabalin

NDC 47335-691 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091157
Dosage form / routeCAPSULE · ORAL
Active ingredientsPREGABALIN (200 mg/1)
Marketing started20191204
Package count4

External sources

Source: openFDA. Public-domain (CC0).