Package 43742-1489-1

Brand: norepinephrine

Generic: norepinephrine (bitartrate)
NDC Package

Package Facts

Identity

Package NDC 43742-1489-1
Digits Only 4374214891
Product NDC 43742-1489
Description

30 mL in 1 BOTTLE, DROPPER (43742-1489-1)

Marketing

Marketing Status
Marketed Since 2019-05-28
Brand norepinephrine
Generic norepinephrine (bitartrate)
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a61e9472-9464-4461-a331-5a0c8d8c8b58", "openfda": {"unii": ["IFY5PE3ZRW"], "spl_set_id": ["8dea9818-e3f1-4c51-9e67-83a63f3e950c"], "manufacturer_name": ["Deseret Biologicals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, DROPPER (43742-1489-1)", "package_ndc": "43742-1489-1", "marketing_start_date": "20190528"}], "brand_name": "Norepinephrine", "product_id": "43742-1489_a61e9472-9464-4461-a331-5a0c8d8c8b58", "dosage_form": "LIQUID", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "43742-1489", "generic_name": "Norepinephrine (Bitartrate)", "labeler_name": "Deseret Biologicals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Norepinephrine", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "8 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20190528", "listing_expiration_date": "20261231"}