tizanidine

Product NDC
60760-503
11-digit product format
607600503
Labeler code
60760
Product ID
60760-503_7b2f41ec-06ce-4d1f-e053-2991aa0a0512
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
2015-12-03
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

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
60760-503-04607600503044 TABLET in 1 BOTTLE, PLASTIC (60760-503-04) 4 tablet2018-03-060000-00-00NoNoCurrent
60760-503-106076005031010 TABLET in 1 BOTTLE, PLASTIC (60760-503-10) 10 tablet2018-03-060000-00-00NoNoCurrent
60760-503-156076005031515 TABLET in 1 BOTTLE, PLASTIC (60760-503-15) 15 tablet2015-12-030000-00-00NoNoCurrent
60760-503-306076005033030 TABLET in 1 BOTTLE, PLASTIC (60760-503-30) 30 tablet2017-02-150000-00-00NoNoCurrent
60760-503-606076005036060 TABLET in 1 BOTTLE, PLASTIC (60760-503-60) 60 tablet2016-02-240000-00-00NoNoCurrent
60760-503-906076005039090 TABLET in 1 BOTTLE, PLASTIC (60760-503-90) 90 tablet2016-04-040000-00-00NoNoCurrent