Package 70518-3702-1

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3702-1
Digits Only 7051837021
Product NDC 70518-3702
Product ID 70518-3702_4c1fdb46-223c-2c56-e063-6394a90a5c84
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3702-1)

Marketing

Marketing Status
Marketed Since 2023-04-12
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": "4c1fdb46-223c-2c56-e063-6394a90a5c84", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["51d85ea8-8317-4a76-a108-20383f118ad4"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3702-1)", "package_ndc": "70518-3702-1", "marketing_start_date": "20230412"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "70518-3702_4c1fdb46-223c-2c56-e063-6394a90a5c84", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-3702", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "REMEDYREPACK 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": "20230406", "listing_expiration_date": "20271231"}