Package 71288-439-05

Brand: norepinephrine bitartrate

Generic: norepinephrine bitartrate
NDC Package

Package Facts

Identity

Package NDC 71288-439-05
Digits Only 7128843905
Product NDC 71288-439
Description

10 VIAL, SINGLE-USE in 1 CARTON (71288-439-05) / 4 mL in 1 VIAL, SINGLE-USE (71288-439-04)

Marketing

Marketing Status
Marketed Since 2024-12-01
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": "48ca273a-3c9d-4466-8804-a0a24790d379", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["53578ac5-b510-4698-a097-f785bfea9fc0"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (71288-439-05)  / 4 mL in 1 VIAL, SINGLE-USE (71288-439-04)", "package_ndc": "71288-439-05", "marketing_start_date": "20241201"}], "brand_name": "Norepinephrine Bitartrate", "product_id": "71288-439_48ca273a-3c9d-4466-8804-a0a24790d379", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "71288-439", "generic_name": "Norepinephrine Bitartrate", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norepinephrine Bitartrate", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA040455", "marketing_category": "ANDA", "marketing_start_date": "20241201", "listing_expiration_date": "20261231"}