cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride

Labeler: medsource pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

cyclobenzaprine hydrochloride 10 mg/1

Manufacturer
Medsource Pharmaceuticals

Identifiers & Regulatory

Product NDC 45865-244
Product ID 45865-244_12645512-7cb8-0532-e063-6294a90acbe5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078643
Listing Expiration 2026-12-31
Marketing Start 2008-09-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 45865244
Hyphenated Format 45865-244

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 ANDA078643 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 14 TABLET, FILM COATED in 1 BOTTLE (45865-244-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE (45865-244-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (45865-244-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (45865-244-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (45865-244-90)
source: ndc

Packages (5)

45865-244-14 14 TABLET, FILM COATED in 1 BOTTLE (45865-244-14) 45865-244-20 20 TABLET, FILM COATED in 1 BOTTLE (45865-244-20) 45865-244-30 30 TABLET, FILM COATED in 1 BOTTLE (45865-244-30) 45865-244-60 60 TABLET, FILM COATED in 1 BOTTLE (45865-244-60) 45865-244-90 90 TABLET, FILM COATED in 1 BOTTLE (45865-244-90)

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": "12645512-7cb8-0532-e063-6294a90acbe5", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["12645f19-fffc-8b08-e063-6394a90a5c55"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (45865-244-14)", "package_ndc": "45865-244-14", "marketing_start_date": "20230307"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (45865-244-20)", "package_ndc": "45865-244-20", "marketing_start_date": "20230710"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (45865-244-30)", "package_ndc": "45865-244-30", "marketing_start_date": "20230523"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (45865-244-60)", "package_ndc": "45865-244-60", "marketing_start_date": "20230223"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (45865-244-90)", "package_ndc": "45865-244-90", "marketing_start_date": "20230223"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "45865-244_12645512-7cb8-0532-e063-6294a90acbe5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "45865-244", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Medsource Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20080926", "listing_expiration_date": "20261231"}