Tizanidine

Product NDC
60760-263
11-digit product format
607600263
Labeler code
60760
Product ID
60760-263_8abd00cd-9256-da09-e053-2995a90aa39c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tizanidine
Dosage form
TABLET
Route
ORAL
Labeler
St. Mary's Medical Park Pharmacy
Application
ANDA091283
Marketing category
ANDA
Marketing start
2018-07-19
Marketing end
0000-00-00
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
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60760-263-04607600263044 TABLET in 1 BOTTLE, PLASTIC (60760-263-04) 4 tablet2019-05-170000-00-00NoNoCurrent
60760-263-156076002631515 TABLET in 1 BOTTLE, PLASTIC (60760-263-15) 15 tablet2018-07-190000-00-00NoNoCurrent
60760-263-306076002633030 TABLET in 1 BOTTLE, PLASTIC (60760-263-30) 30 tablet2018-08-210000-00-00NoNoCurrent
60760-263-606076002636060 TABLET in 1 BOTTLE, PLASTIC (60760-263-60) 60 tablet2019-06-070000-00-00NoNoCurrent
60760-263-906076002639090 TABLET in 1 BOTTLE, PLASTIC (60760-263-90) 90 tablet2018-09-050000-00-00NoNoCurrent