tizanidine hydrochloride

Product NDC
71335-2872
11-digit product format
713352872
Labeler code
71335
Product ID
71335-2872_e8dc9434-dcbd-4d1a-9ac2-6c29d7f88477
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
tizanidine hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA213798
Marketing category
ANDA
Marketing start
2020-05-27
Substance
TIZANIDINE HYDROCHLORIDE
Active strength
6 mg/1
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
B53E3NMY5CTIZANIDINE HYDROCHLORIDE64461-82-1TIZANIDINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2872-17133528720130 CAPSULE in 1 BOTTLE (71335-2872-1) 30 capsule2025-10-28NoNoHistorical
71335-2872-27133528720260 CAPSULE in 1 BOTTLE (71335-2872-2) 60 capsule2025-10-28NoNoHistorical
71335-2872-37133528720390 CAPSULE in 1 BOTTLE (71335-2872-3) 90 capsule2025-10-28NoNoHistorical
71335-2872-471335287204120 CAPSULE in 1 BOTTLE (71335-2872-4) 120 capsule2025-10-28NoNoHistorical
71335-2872-57133528720528 CAPSULE in 1 BOTTLE (71335-2872-5) 28 capsule2025-10-28NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
tizanidine hydrochlorideBryant Ranch Prepack2025-10-28HUMAN PRESCRIPTION DRUG LABEL1