TIZANIDINE

Product NDC

49884-773

11-digit product format

498840773

Labeler code

49884

Product ID

49884-773_549c2df9-d1ec-4e47-8bae-d34e3a156391

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

TIZANIDINE

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical, Inc.

Application

ANDA207170

Marketing category

ANDA

Marketing start

2017-01-17

Marketing end

2019-07-31

Substance

TIZANIDINE HYDROCHLORIDE

Active strength

4 mg/1

Pharmacologic classes

Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record