tizanidine hydrochloride
Generic: tizanidine hydrochloride
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
tizanidine hydrochloride
Generic Name
tizanidine hydrochloride
Labeler
aurobindo pharma limited
Dosage Form
CAPSULE
Routes
Active Ingredients
tizanidine hydrochloride 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59651-314
Product ID
59651-314_c5462b0a-179b-449f-87e9-1ccfa18367b3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213544
Listing Expiration
2026-12-31
Marketing Start
2020-03-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59651314
Hyphenated Format
59651-314
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 hydrochloride (source: ndc)
Generic Name
tizanidine hydrochloride (source: ndc)
Application Number
ANDA213544 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 150 CAPSULE in 1 BOTTLE (59651-314-77)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c5462b0a-179b-449f-87e9-1ccfa18367b3", "openfda": {"unii": ["B53E3NMY5C"], "rxcui": ["485484", "485485", "485486"], "spl_set_id": ["19cf46b5-d8dc-44cb-83d6-bacea0870dbe"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 CAPSULE in 1 BOTTLE (59651-314-77)", "package_ndc": "59651-314-77", "marketing_start_date": "20200324"}], "brand_name": "Tizanidine Hydrochloride", "product_id": "59651-314_c5462b0a-179b-449f-87e9-1ccfa18367b3", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "59651-314", "generic_name": "Tizanidine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tizanidine Hydrochloride", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA213544", "marketing_category": "ANDA", "marketing_start_date": "20200324", "listing_expiration_date": "20261231"}