FDA NDC Directory · JSON-LD · Markdown

Minocycline Hydrochloride

NDC 57664-853 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090867
Dosage form / routeCAPSULE · ORAL
Active ingredientsMINOCYCLINE HYDROCHLORIDE (100 mg/1)
Marketing started20130513
Package count2

External sources

Source: openFDA. Public-domain (CC0).