Minocycline Hydrochloride

Product NDC

0093-7742

11-digit product format

000937742

Labeler code

0093

Product ID

0093-7742_b88f4b72-9c50-4aca-9593-2b77be65b36e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline Hydrochloride

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA065485

Marketing category

ANDA

Marketing start

2019-02-19

Marketing end

2021-01-31

Substance

MINOCYCLINE HYDROCHLORIDE

Active strength

80 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record