Minocycline Hydrochloride

Product NDC

50090-0635

11-digit product format

500900635

Labeler code

50090

Product ID

50090-0635_5b06439f-84a8-47a0-ab3b-ca4863a419cc

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA063065

Marketing category

ANDA

Marketing start

1993-05-01

Marketing end

0000-00-00

Substance

MINOCYCLINE HYDROCHLORIDE

Active strength

100 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