Package 0781-3755-95

Brand: norepinephrine bitartrate

Generic: norepinephrine bitartrate
NDC Package

Package Facts

Identity

Package NDC 0781-3755-95
Digits Only 0781375595
Product NDC 0781-3755
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3755-95) / 4 mL in 1 VIAL, SINGLE-DOSE (0781-3755-75)

Marketing

Marketing Status
Marketed Since 2019-04-23
Brand norepinephrine bitartrate
Generic norepinephrine bitartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "eaf2eebc-d694-f15a-e053-2995a90a81b6", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["728734e7-1684-4b37-980c-f1dfd408b436"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3755-95)  / 4 mL in 1 VIAL, SINGLE-DOSE (0781-3755-75)", "package_ndc": "0781-3755-95", "marketing_start_date": "20190423"}], "brand_name": "NOREPINEPHRINE BITARTRATE", "product_id": "0781-3755_eaf2eebc-d694-f15a-e053-2995a90a81b6", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "0781-3755", "generic_name": "Norepinephrine Bitartrate", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NOREPINEPHRINE BITARTRATE", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA211359", "marketing_category": "ANDA", "marketing_start_date": "20190423", "listing_expiration_date": "20261231"}