FDA NDC Directory · JSON-LD · Markdown

Minocin

NDC 70842-160 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameminocycline hydrochloride
Labeler / ManufacturerMelinta Therapeutics, LLC
Marketing categoryNew Drug Application (innovator) · App NDA050444
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsMINOCYCLINE HYDROCHLORIDE (100 mg/1)
Marketing started20130419
Package count1

External sources

Source: openFDA. Public-domain (CC0).