Minocycline Hydrochloride

Product NDC

68788-6997

11-digit product format

687886997

Labeler code

68788

Product ID

68788-6997_8497bd3f-832b-4648-bc5d-d2533e59989f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA090867

Marketing category

ANDA

Marketing start

2017-07-24

Marketing end

0000-00-00

Substance

MINOCYCLINE HYDROCHLORIDE

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record