Package 70518-3251-2

Brand: cyclobenzaprine hydrochloride

Generic: cyclobenzaprine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3251-2
Digits Only 7051832512
Product NDC 70518-3251
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3251-2)

Marketing

Marketing Status
Marketed Since 2021-11-23
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": "40cddbcb-5378-24e9-e063-6394a90ad7d2", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["eb2b24b1-2851-440f-9075-b6a123a1fd5c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3251-2)", "package_ndc": "70518-3251-2", "marketing_start_date": "20211123"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-5)", "package_ndc": "70518-3251-5", "marketing_start_date": "20230228"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-6)", "package_ndc": "70518-3251-6", "marketing_start_date": "20250609"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "70518-3251_40cddbcb-5378-24e9-e063-6394a90ad7d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-3251", "generic_name": "Cyclobenzaprine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20211020", "listing_expiration_date": "20261231"}