Demeclocycline Hydrochloride

Product NDC

0555-0702

11-digit product format

005550702

Labeler code

0555

Product ID

0555-0702_154e0e1c-1193-4ce2-8c31-a8c3e34f469a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Demeclocycline Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA065171

Marketing category

ANDA

Marketing start

2005-01-04

Marketing end

0000-00-00

Substance

DEMECLOCYCLINE HYDROCHLORIDE

Active strength

300 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record