Package 47335-615-44

Brand: norepinephrine bitartrate

Generic: norepinephrine bitartrate
NDC Package

Package Facts

Identity

Package NDC 47335-615-44
Digits Only 4733561544
Product NDC 47335-615
Product ID 47335-615_4bb42f07-a41e-42f3-92e7-dab665584f84
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (47335-615-44) / 4 mL in 1 VIAL, SINGLE-DOSE

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": "4bb42f07-a41e-42f3-92e7-dab665584f84", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["4bb42f07-a41e-42f3-92e7-dab665584f84"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (47335-615-44)  / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "47335-615-44", "marketing_start_date": "20210701"}], "brand_name": "NOREPINEPHRINE BITARTRATE", "product_id": "47335-615_4bb42f07-a41e-42f3-92e7-dab665584f84", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "47335-615", "generic_name": "NOREPINEPHRINE BITARTRATE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NOREPINEPHRINE BITARTRATE", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA211980", "marketing_category": "ANDA", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}