cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride

Labeler: sportpharm llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclobenzaprine hydrochloride
Generic Name cyclobenzaprine hydrochloride
Labeler sportpharm llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cyclobenzaprine hydrochloride 10 mg/1

Manufacturer
Sportpharm LLC

Identifiers & Regulatory

Product NDC 85766-003
Product ID 85766-003_4a8f971b-ad9c-5c85-e063-6394a90a9aff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208170
Listing Expiration 2027-12-31
Marketing Start 2017-05-31

Pharmacologic Class

Classes
centrally-mediated muscle relaxation [pe] muscle relaxant [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 85766003
Hyphenated Format 85766-003

Supplemental Identifiers

RxCUI
828348
UNII
0VE05JYS2P

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 ANDA208170 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (85766-003-00)
  • 1 TABLET, FILM COATED in 1 BOTTLE (85766-003-01)
  • 2 TABLET, FILM COATED in 1 BOTTLE (85766-003-02)
  • 4 TABLET, FILM COATED in 1 BOTTLE (85766-003-04)
  • 5 TABLET, FILM COATED in 1 BOTTLE (85766-003-05)
  • 7 TABLET, FILM COATED in 1 BOTTLE (85766-003-07)
  • 100 TABLET, FILM COATED in 1 BOTTLE (85766-003-10)
  • 14 TABLET, FILM COATED in 1 BOTTLE (85766-003-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE (85766-003-20)
  • 21 TABLET, FILM COATED in 1 BOTTLE (85766-003-21)
  • 30 TABLET, FILM COATED in 1 BOTTLE (85766-003-30)
  • 500 TABLET, FILM COATED in 1 BOTTLE (85766-003-50)
  • 60 TABLET, FILM COATED in 1 BOTTLE (85766-003-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (85766-003-90)
source: ndc

Packages (14)

85766-003-00 1000 TABLET, FILM COATED in 1 BOTTLE (85766-003-00) 85766-003-01 1 TABLET, FILM COATED in 1 BOTTLE (85766-003-01) 85766-003-02 2 TABLET, FILM COATED in 1 BOTTLE (85766-003-02) 85766-003-04 4 TABLET, FILM COATED in 1 BOTTLE (85766-003-04) 85766-003-05 5 TABLET, FILM COATED in 1 BOTTLE (85766-003-05) 85766-003-07 7 TABLET, FILM COATED in 1 BOTTLE (85766-003-07) 85766-003-10 100 TABLET, FILM COATED in 1 BOTTLE (85766-003-10) 85766-003-14 14 TABLET, FILM COATED in 1 BOTTLE (85766-003-14) 85766-003-20 20 TABLET, FILM COATED in 1 BOTTLE (85766-003-20) 85766-003-21 21 TABLET, FILM COATED in 1 BOTTLE (85766-003-21) 85766-003-30 30 TABLET, FILM COATED in 1 BOTTLE (85766-003-30) 85766-003-50 500 TABLET, FILM COATED in 1 BOTTLE (85766-003-50) 85766-003-60 60 TABLET, FILM COATED in 1 BOTTLE (85766-003-60) 85766-003-90 90 TABLET, FILM COATED in 1 BOTTLE (85766-003-90)

Ingredients (1)

cyclobenzaprine hydrochloride (10 mg/1)

Linked Drug Pages (1)

CYCLOBENZAPRINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a8f971b-ad9c-5c85-e063-6394a90a9aff", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["d4e0f532-887b-40bb-80d6-5c4e5b1d64bf"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (85766-003-00)", "package_ndc": "85766-003-00", "marketing_start_date": "20250620"}, {"sample": false, "description": "1 TABLET, FILM COATED in 1 BOTTLE (85766-003-01)", "package_ndc": "85766-003-01", "marketing_start_date": "20250620"}, {"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (85766-003-02)", "package_ndc": "85766-003-02", "marketing_start_date": "20250620"}, {"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (85766-003-04)", "package_ndc": "85766-003-04", "marketing_start_date": "20250620"}, {"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE (85766-003-05)", "package_ndc": "85766-003-05", "marketing_start_date": "20250620"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (85766-003-07)", "package_ndc": "85766-003-07", "marketing_start_date": "20250620"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (85766-003-10)", "package_ndc": "85766-003-10", "marketing_start_date": "20250620"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (85766-003-14)", "package_ndc": "85766-003-14", "marketing_start_date": "20260211"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (85766-003-20)", "package_ndc": "85766-003-20", "marketing_start_date": "20250620"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (85766-003-21)", "package_ndc": "85766-003-21", "marketing_start_date": "20260211"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85766-003-30)", "package_ndc": "85766-003-30", "marketing_start_date": "20250620"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (85766-003-50)", "package_ndc": "85766-003-50", "marketing_start_date": "20250620"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85766-003-60)", "package_ndc": "85766-003-60", "marketing_start_date": "20250620"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85766-003-90)", "package_ndc": "85766-003-90", "marketing_start_date": "20250620"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "85766-003_4a8f971b-ad9c-5c85-e063-6394a90a9aff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "85766-003", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Sportpharm LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20271231"}