Package 0904-7400-06

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7400-06
Digits Only 0904740006
Product NDC 0904-7400
Product ID 0904-7400_01d0daef-106b-4557-95d2-380a993ba9f1
Description

50 BLISTER PACK in 1 CARTON (0904-7400-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2027-01-31
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Cyclobenzaprine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "01d0daef-106b-4557-95d2-380a993ba9f1", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["508e310e-067a-4f95-869a-e1da49aabe94"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-7400-04)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7400-04", "marketing_end_date": "20270131", "marketing_start_date": "20240221"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7400-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7400-06", "marketing_end_date": "20270131", "marketing_start_date": "20240221"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "0904-7400_01d0daef-106b-4557-95d2-380a993ba9f1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "0904-7400", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20080926"}