Tindazole

Product NDC

16571-215

11-digit product format

165710215

Labeler code

16571

Product ID

16571-215_3a66b537-63a4-41f9-8415-5ed05bd8cbcf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tinidazole

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Pack Pharmaceuticals, LLC

Application

ANDA202489

Marketing category

ANDA

Marketing start

2013-10-09

Marketing end

0000-00-00

Substance

TINIDAZOLE

Active strength

500 mg/1

Pharmacologic classes

Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record