tizanidine
Generic: tizanidine
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
tizanidine
Generic Name
tizanidine
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
tizanidine hydrochloride 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4181
Product ID
70518-4181_3ff1afa9-91d2-aab5-e063-6394a90a28d0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208187
Listing Expiration
2026-12-31
Marketing Start
2024-09-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184181
Hyphenated Format
70518-4181
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
ANDA208187 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-4181-0)
- 30 TABLET in 1 BOTTLE, PLASTIC (70518-4181-1)
- 30 TABLET in 1 BLISTER PACK (70518-4181-2)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ff1afa9-91d2-aab5-e063-6394a90a28d0", "openfda": {"unii": ["B53E3NMY5C"], "rxcui": ["313413"], "spl_set_id": ["63b7eba3-6dea-4d89-bc42-7e965ae9795d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4181-0)", "package_ndc": "70518-4181-0", "marketing_start_date": "20240923"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-4181-1)", "package_ndc": "70518-4181-1", "marketing_start_date": "20241030"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4181-2)", "package_ndc": "70518-4181-2", "marketing_start_date": "20250810"}], "brand_name": "tizanidine", "product_id": "70518-4181_3ff1afa9-91d2-aab5-e063-6394a90a28d0", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]"], "product_ndc": "70518-4181", "generic_name": "tizanidine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tizanidine", "active_ingredients": [{"name": "TIZANIDINE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA208187", "marketing_category": "ANDA", "marketing_start_date": "20240923", "listing_expiration_date": "20261231"}