Package 70377-121-12

Brand: norepinephrine bitartrate

Generic: norepinephrine bitartrate
NDC Package

Package Facts

Identity

Package NDC 70377-121-12
Digits Only 7037712112
Product NDC 70377-121
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (70377-121-12) / 4 mL in 1 VIAL, SINGLE-DOSE (70377-121-11)

Marketing

Marketing Status
Marketed Since 2025-07-01
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": "240616bf-5277-ae18-dc3d-738f3bbabb55", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["0ea48ab6-e166-df31-b132-70ef982a2d02"], "manufacturer_name": ["BIOCON PHARMA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (70377-121-12)  / 4 mL in 1 VIAL, SINGLE-DOSE (70377-121-11)", "package_ndc": "70377-121-12", "marketing_start_date": "20250701"}], "brand_name": "NOREPINEPHRINE BITARTRATE", "product_id": "70377-121_240616bf-5277-ae18-dc3d-738f3bbabb55", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "70377-121", "generic_name": "NOREPINEPHRINE BITARTRATE", "labeler_name": "BIOCON PHARMA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NOREPINEPHRINE BITARTRATE", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA219443", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}