FDA NDC Directory · JSON-LD · Markdown

Minocycline Hydrochloride

NDC 68788-7052 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065470
Dosage form / routeCAPSULE · ORAL
Active ingredientsMINOCYCLINE HYDROCHLORIDE (100 mg/1)
Marketing started20171106
Package count3

External sources

Source: openFDA. Public-domain (CC0).