cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cyclobenzaprine hydrochloride
Generic Name cyclobenzaprine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cyclobenzaprine hydrochloride 7.5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1848
Product ID 50090-1848_1152b0be-6787-461b-bf78-695595c2c63b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078722
Listing Expiration 2026-12-31
Marketing Start 2015-03-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901848
Hyphenated Format 50090-1848

Supplemental Identifiers

RxCUI
828299
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 ANDA078722 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 7.5 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BOTTLE (50090-1848-0)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-1848-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-1848-2)
source: ndc

Packages (3)

50090-1848-0 15 TABLET, FILM COATED in 1 BOTTLE (50090-1848-0) 50090-1848-1 30 TABLET, FILM COATED in 1 BOTTLE (50090-1848-1) 50090-1848-2 60 TABLET, FILM COATED in 1 BOTTLE (50090-1848-2)

Ingredients (1)

cyclobenzaprine hydrochloride (7.5 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": "1152b0be-6787-461b-bf78-695595c2c63b", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["81917fa4-c79c-46e2-bfbb-507fc0d7ed1b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-1848-0)", "package_ndc": "50090-1848-0", "marketing_start_date": "20150528"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-1848-1)", "package_ndc": "50090-1848-1", "marketing_start_date": "20150528"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-1848-2)", "package_ndc": "50090-1848-2", "marketing_start_date": "20150528"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "50090-1848_1152b0be-6787-461b-bf78-695595c2c63b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-1848", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078722", "marketing_category": "ANDA", "marketing_start_date": "20150325", "listing_expiration_date": "20261231"}