Minocycline Hydrochloride

Product NDC

70518-0359

11-digit product format

705180359

Labeler code

70518

Product ID

70518-0359_7f86bf5f-5cd7-1f6f-e053-2991aa0a2fbf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA065436

Marketing category

ANDA

Marketing start

2017-04-27

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