Minocin

Product NDC

16781-400

11-digit product format

167810400

Labeler code

16781

Product ID

16781-400_bdd0be98-5e2c-4115-a434-3eced718541e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

minocycline hydrochloride

Dosage form

CAPSULE, COATED PELLETS

Route

ORAL

Labeler

Bausch Health US, LLC

Application

NDA050649

Marketing category

NDA

Marketing start

1990-05-31

Marketing end

0000-00-00

Substance

MINOCYCLINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

Tetracycline-class Drug [EPC],Tetracyclines [CS]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record