FDA NDC Directory · JSON-LD · Markdown

QUININE SULFATE

NDC 68180-560 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203112
Dosage form / routeCAPSULE · ORAL
Active ingredientsQUININE SULFATE (324 mg/1)
Marketing started20150804
Package count1

External sources

Source: openFDA. Public-domain (CC0).