Minocycline Hydrochloride

Product NDC

68071-3307

11-digit product format

680713307

Labeler code

68071

Product ID

68071-3307_5034abdf-e5ec-5057-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA090867

Marketing category

ANDA

Marketing start

2013-05-13

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

2020-12-31

Current FDA listing

Historical FDA.report record