Package 68071-3404-3

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3404-3
Digits Only 6807134043
Product NDC 68071-3404
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-3404-3)

Marketing

Marketing Status
Marketed Since 2023-05-16
Brand cyclobenzaprine hydrochloride
Generic cyclobenzaprine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d5414d9-c9c8-6bbd-e063-6294a90a976c", "openfda": {"upc": ["0368071340433"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["fbd38abb-02ae-1a36-e053-6294a90abe65"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3404-3)", "package_ndc": "68071-3404-3", "marketing_start_date": "20230516"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "68071-3404_2d5414d9-c9c8-6bbd-e063-6294a90a976c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-3404", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}