tizanidine

Product NDC
60760-253
11-digit product format
607600253
Labeler code
60760
Product ID
60760-253_d27f27fe-76fe-a220-e053-2995a90af29f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tizanidine
Dosage form
TABLET
Route
ORAL
Labeler
St. Mary's Medical Park Pharmacy
Application
ANDA076533
Marketing category
ANDA
Marketing start
2004-01-16
Marketing end
0000-00-00
Substance
TIZANIDINE HYDROCHLORIDE
Active strength
2 mg/1
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
B53E3NMY5CTIZANIDINE HYDROCHLORIDE64461-82-1TIZANIDINE HYDROCHLORIDE
6AI06C00GWTIZANIDINE51322-75-9tizanidine

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60760-253-04607600253044 TABLET in 1 BOTTLE, PLASTIC (60760-253-04) 4 tablet2018-03-050000-00-00NoNoCurrent
60760-253-106076002531010 TABLET in 1 BOTTLE, PLASTIC (60760-253-10) 10 tablet2018-03-050000-00-00NoNoCurrent
60760-253-156076002531515 TABLET in 1 BOTTLE, PLASTIC (60760-253-15) 15 tablet2017-11-170000-00-00NoNoCurrent
60760-253-306076002533030 TABLET in 1 BOTTLE, PLASTIC (60760-253-30) 30 tablet2017-11-170000-00-00NoNoCurrent
60760-253-906076002539090 TABLET in 1 BOTTLE, PLASTIC (60760-253-90) 90 tablet2017-11-170000-00-00NoNoCurrent