cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
cyclobenzaprine hydrochloride
Generic Name
cyclobenzaprine hydrochloride
Labeler
remedyrepack inc.
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
cyclobenzaprine hydrochloride 15 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4225
Product ID
70518-4225_4004e5c0-1ec3-9534-e063-6294a90a068a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091281
Listing Expiration
2026-12-31
Marketing Start
2024-10-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184225
Hyphenated Format
70518-4225
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
cyclobenzaprine hydrochloride (source: ndc)
Generic Name
cyclobenzaprine hydrochloride (source: ndc)
Application Number
ANDA091281 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 mg/1
Packaging
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4225-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4004e5c0-1ec3-9534-e063-6294a90a068a", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828358"], "spl_set_id": ["ba659e1a-0091-45f6-b418-f4f36c9a2c79"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4225-0)", "package_ndc": "70518-4225-0", "marketing_start_date": "20241031"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "70518-4225_4004e5c0-1ec3-9534-e063-6294a90a068a", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-4225", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA091281", "marketing_category": "ANDA", "marketing_start_date": "20241031", "listing_expiration_date": "20261231"}