Minocycline hydrochloride

Product NDC

50090-0633

11-digit product format

500900633

Labeler code

50090

Product ID

50090-0633_ae1f9917-152a-4fbd-8409-6921b416b826

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA065062

Marketing category

ANDA

Marketing start

2000-12-22

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

2019-12-31

Current FDA listing

Historical FDA.report record