cyclobenzaprine hydrochloride
Generic: cyclobenzaprine hydrochloride
Labeler: avpakDrug Facts
Product Profile
Brand Name
cyclobenzaprine hydrochloride
Generic Name
cyclobenzaprine hydrochloride
Labeler
avpak
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cyclobenzaprine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-190
Product ID
50268-190_423d93a8-e8b9-b8a0-e063-6294a90a73be
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090478
Listing Expiration
2026-12-31
Marketing Start
2014-06-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268190
Hyphenated Format
50268-190
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
ANDA090478 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 50 BLISTER PACK in 1 BOX (50268-190-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-190-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "423d93a8-e8b9-b8a0-e063-6294a90a73be", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["64f6d1be-4067-a5c7-2343-4aed651a0cac"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-190-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-190-11)", "package_ndc": "50268-190-15", "marketing_start_date": "20140610"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "50268-190_423d93a8-e8b9-b8a0-e063-6294a90a73be", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50268-190", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090478", "marketing_category": "ANDA", "marketing_start_date": "20140610", "listing_expiration_date": "20261231"}