Package 72078-002-04

Brand: norepinephrine bitartrate

Generic: norepinephrine bitartrate
NDC Package

Package Facts

Identity

Package NDC 72078-002-04
Digits Only 7207800204
Product NDC 72078-002
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (72078-002-04) / 4 mL in 1 VIAL, SINGLE-DOSE (72078-002-00)

Marketing

Marketing Status
Marketed Since 2020-12-04
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": "f55bd465-c5b2-4542-8765-00480fd6043d", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["7a4950ea-6369-4dd5-97be-df21a5a5055f"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72078-002-04)  / 4 mL in 1 VIAL, SINGLE-DOSE (72078-002-00)", "package_ndc": "72078-002-04", "marketing_start_date": "20201204"}], "brand_name": "Norepinephrine bitartrate", "product_id": "72078-002_f55bd465-c5b2-4542-8765-00480fd6043d", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "72078-002", "generic_name": "Norepinephrine bitartrate", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norepinephrine bitartrate", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA211242", "marketing_category": "ANDA", "marketing_start_date": "20201204", "listing_expiration_date": "20261231"}