FDA NDC Directory · JSON-LD · Markdown

Minocycline hydrochloride

NDC 68382-317 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA063009
Dosage form / routeCAPSULE · ORAL
Active ingredientsMINOCYCLINE HYDROCHLORIDE (75 mg/1)
Marketing started20170403
Package count1

External sources

Source: openFDA. Public-domain (CC0).