Package 83854-017-10
Brand: norepinephrine bitartrate
Generic: norepinephrine bitartratePackage Facts
Identity
Package NDC
83854-017-10
Digits Only
8385401710
Product NDC
83854-017
Description
10 VIAL in 1 CARTON (83854-017-10) / 4 mL in 1 VIAL (83854-017-01)
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": "44791190-e870-ac45-e063-6294a90acaa9", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["52e22892-4fc3-4f53-9f39-0b5c66da3040"], "manufacturer_name": ["Anthea Pharma Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (83854-017-10) / 4 mL in 1 VIAL (83854-017-01)", "package_ndc": "83854-017-10", "marketing_start_date": "20251125"}], "brand_name": "NOREPINEPHRINE BITARTRATE", "product_id": "83854-017_44791190-e870-ac45-e063-6294a90acaa9", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "83854-017", "generic_name": "NOREPINEPHRINE BITARTRATE", "labeler_name": "Anthea Pharma Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NOREPINEPHRINE BITARTRATE", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA219924", "marketing_category": "ANDA", "marketing_start_date": "20251125", "listing_expiration_date": "20261231"}