Package 0338-0112-20
Brand: norepinephrine bitartrate
Generic: norepinephrine bitartratePackage Facts
Identity
Package NDC
0338-0112-20
Digits Only
0338011220
Product NDC
0338-0112
Description
20 BAG in 1 CARTON (0338-0112-20) / 250 mL in 1 BAG
Marketing
Marketing Status
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": "b40627c0-67bf-4740-9d21-83054aa6afd9", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["2475337", "2475340", "2619579"], "spl_set_id": ["6363e9b4-29df-4553-904d-a563e5adda6e"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BAG in 1 CARTON (0338-0112-20) / 250 mL in 1 BAG", "package_ndc": "0338-0112-20", "marketing_start_date": "20210115"}], "brand_name": "NOREPINEPHRINE BITARTRATE", "product_id": "0338-0112_b40627c0-67bf-4740-9d21-83054aa6afd9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "0338-0112", "generic_name": "norepinephrine bitartrate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NOREPINEPHRINE BITARTRATE", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "4 mg/250mL"}], "application_number": "NDA214313", "marketing_category": "NDA", "marketing_start_date": "20210115", "listing_expiration_date": "20271231"}