Minocycline Hydrochloride

Product NDC

50436-0108

11-digit product format

504360108

Labeler code

50436

Product ID

50436-0108_edbdc0b0-b98a-47c0-a370-4b55d29dc8d6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA065470

Marketing category

ANDA

Marketing start

2008-03-11

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