Package 36000-162-10

Brand: norepinephrine bitartrate

Generic: norepinephrine bitartrate
NDC Package

Package Facts

Identity

Package NDC 36000-162-10
Digits Only 3600016210
Product NDC 36000-162
Product ID 36000-162_73f5f4bb-09e2-4c5f-b482-c960bb957d53
Description

10 AMPULE in 1 CARTON (36000-162-10) / 4 mL in 1 AMPULE (36000-162-01)

Marketing

Marketing Status
Marketed Since 2012-04-01
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": "73f5f4bb-09e2-4c5f-b482-c960bb957d53", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["a27fb6e0-8f7a-11db-9739-0050c2490048"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (36000-162-10)  / 4 mL in 1 AMPULE (36000-162-01)", "package_ndc": "36000-162-10", "marketing_start_date": "20120401"}], "brand_name": "Norepinephrine bitartrate", "product_id": "36000-162_73f5f4bb-09e2-4c5f-b482-c960bb957d53", "dosage_form": "INJECTION", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "36000-162", "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": "1 mg/mL"}], "application_number": "ANDA040859", "marketing_category": "ANDA", "marketing_start_date": "20120401", "listing_expiration_date": "20261231"}