tizanidine hydrochloride
Generic: tizanidine hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
tizanidine hydrochloride
Generic Name
tizanidine hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
tizanidine hydrochloride 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-506
Product ID
72789-506_354616bb-6b9a-4328-e063-6294a90a7063
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213798
Listing Expiration
2026-12-31
Marketing Start
2020-05-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789506
Hyphenated Format
72789-506
Supplemental Identifiers
RxCUI
UPC
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 hydrochloride (source: ndc)
Generic Name
tizanidine hydrochloride (source: ndc)
Application Number
ANDA213798 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/1
Packaging
- 150 CAPSULE in 1 BOTTLE, PLASTIC (72789-506-77)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "354616bb-6b9a-4328-e063-6294a90a7063", "openfda": {"upc": ["0372789506777"], "unii": ["B53E3NMY5C"], "rxcui": ["485486"], "spl_set_id": ["e94aa8b1-74ed-46b7-94c5-53d5d5630be6"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "150 CAPSULE in 1 BOTTLE, PLASTIC (72789-506-77)", "package_ndc": "72789-506-77", "marketing_start_date": "20250516"}], "brand_name": "tizanidine hydrochloride", "product_id": "72789-506_354616bb-6b9a-4328-e063-6294a90a7063", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "72789-506", "generic_name": "tizanidine hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tizanidine hydrochloride", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA213798", "marketing_category": "ANDA", "marketing_start_date": "20200527", "listing_expiration_date": "20261231"}