Package 25021-316-04

Brand: norepinephrine bitartrate

Generic: norepinephrine bitartrate
NDC Package

Package Facts

Identity

Package NDC 25021-316-04
Digits Only 2502131604
Product NDC 25021-316
Product ID 25021-316_61b38873-cf8d-48b6-b126-2e0a32ac5f7a
Description

10 VIAL in 1 CARTON (25021-316-04) / 4 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2021-07-01
Brand norepinephrine bitartrate
Generic norepinephrine bitartrate
Sample Package No

Linked Drug Pages (1)

Norepinephrine Bitartrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "61b38873-cf8d-48b6-b126-2e0a32ac5f7a", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["cc9ecec5-3bd7-4132-9745-7666bac8ceac"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-316-04)  / 4 mL in 1 VIAL", "package_ndc": "25021-316-04", "marketing_start_date": "20210701"}], "brand_name": "Norepinephrine Bitartrate", "product_id": "25021-316_61b38873-cf8d-48b6-b126-2e0a32ac5f7a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "25021-316", "generic_name": "Norepinephrine Bitartrate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norepinephrine Bitartrate", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA214323", "marketing_category": "ANDA", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}