Package 10702-364-51

Brand: isoproterenol hydrochloride

Generic: isoproterenol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-364-51
Digits Only 1070236451
Product NDC 10702-364
Product ID 10702-364_4391f314-1323-1ec4-e063-6294a90afcbf
Description

10 VIAL in 1 CARTON (10702-364-51) / 5 mL in 1 VIAL (10702-364-05)

Marketing

Marketing Status
Marketed Since 2023-09-25
Brand isoproterenol hydrochloride
Generic isoproterenol hydrochloride
Sample Package No

Linked Drug Pages (1)

Isoproterenol hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "4391f314-1323-1ec4-e063-6294a90afcbf", "openfda": {"unii": ["DIA2A74855"], "rxcui": ["1667915"], "spl_set_id": ["051acbc2-7bf8-4059-e063-6394a90a115b"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (10702-364-51)  / 5 mL in 1 VIAL (10702-364-05)", "package_ndc": "10702-364-51", "marketing_start_date": "20230925"}], "brand_name": "Isoproterenol hydrochloride", "product_id": "10702-364_4391f314-1323-1ec4-e063-6294a90afcbf", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "10702-364", "generic_name": "Isoproterenol hydrochloride", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Isoproterenol hydrochloride", "active_ingredients": [{"name": "ISOPROTERENOL HYDROCHLORIDE", "strength": ".2 mg/mL"}], "application_number": "ANDA215542", "marketing_category": "ANDA", "marketing_start_date": "20230925", "listing_expiration_date": "20261231"}