tizanidine
Generic: tizanidine
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
tizanidine
Generic Name
tizanidine
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
tizanidine hydrochloride 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-5767
Product ID
50090-5767_e68d46ad-efb1-4422-9320-154acf969626
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091283
Listing Expiration
2027-12-31
Marketing Start
2013-04-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500905767
Hyphenated Format
50090-5767
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
tizanidine (source: ndc)
Generic Name
tizanidine (source: ndc)
Application Number
ANDA091283 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (50090-5767-0)
- 60 TABLET in 1 BOTTLE (50090-5767-2)
- 15 TABLET in 1 BOTTLE (50090-5767-3)
- 30 TABLET in 1 BOTTLE (50090-5767-4)
- 90 TABLET in 1 BOTTLE (50090-5767-6)
- 14 TABLET in 1 BOTTLE (50090-5767-7)
Packages (6)
50090-5767-0
120 TABLET in 1 BOTTLE (50090-5767-0)
50090-5767-2
60 TABLET in 1 BOTTLE (50090-5767-2)
50090-5767-3
15 TABLET in 1 BOTTLE (50090-5767-3)
50090-5767-4
30 TABLET in 1 BOTTLE (50090-5767-4)
50090-5767-6
90 TABLET in 1 BOTTLE (50090-5767-6)
50090-5767-7
14 TABLET in 1 BOTTLE (50090-5767-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e68d46ad-efb1-4422-9320-154acf969626", "openfda": {"unii": ["B53E3NMY5C"], "rxcui": ["313413"], "spl_set_id": ["308d2fdc-6136-4e75-95d3-342497add66c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (50090-5767-0)", "package_ndc": "50090-5767-0", "marketing_start_date": "20211004"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-5767-2)", "package_ndc": "50090-5767-2", "marketing_start_date": "20211004"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (50090-5767-3)", "package_ndc": "50090-5767-3", "marketing_start_date": "20211004"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-5767-4)", "package_ndc": "50090-5767-4", "marketing_start_date": "20211004"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-5767-6)", "package_ndc": "50090-5767-6", "marketing_start_date": "20211004"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (50090-5767-7)", "package_ndc": "50090-5767-7", "marketing_start_date": "20211004"}], "brand_name": "Tizanidine", "product_id": "50090-5767_e68d46ad-efb1-4422-9320-154acf969626", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "50090-5767", "generic_name": "Tizanidine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA091283", "marketing_category": "ANDA", "marketing_start_date": "20130401", "listing_expiration_date": "20271231"}