Package 69097-522-35

Brand: isoproterenol

Generic: isoproterenol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69097-522-35
Digits Only 6909752235
Product NDC 69097-522
Description

10 AMPULE in 1 CARTON (69097-522-35) / 5 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2018-06-26
Brand isoproterenol
Generic isoproterenol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRACARDIAC", "INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "6014b0c8-2851-4111-a4f7-6764be850176", "openfda": {"upc": ["0369097521318", "0369097522353"], "unii": ["DIA2A74855"], "rxcui": ["1667909", "1667915"], "spl_set_id": ["f724120d-da28-4065-9e05-d7dd6afbb546"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (69097-522-35)  / 5 mL in 1 AMPULE", "package_ndc": "69097-522-35", "marketing_start_date": "20180626"}], "brand_name": "ISOPROTERENOL", "product_id": "69097-522_6014b0c8-2851-4111-a4f7-6764be850176", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Agonists [MoA]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "69097-522", "generic_name": "isoproterenol hydrochloride", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ISOPROTERENOL", "active_ingredients": [{"name": "ISOPROTERENOL HYDROCHLORIDE", "strength": "1 mg/5mL"}], "application_number": "ANDA210322", "marketing_category": "ANDA", "marketing_start_date": "20180626", "listing_expiration_date": "20261231"}