norepinephrine bitartrate
Generic: norepinephrine bitartrate
Labeler: mylan institutional llcDrug Facts
Product Profile
Brand Name
norepinephrine bitartrate
Generic Name
norepinephrine bitartrate
Labeler
mylan institutional llc
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
norepinephrine bitartrate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72078-002
Product ID
72078-002_f55bd465-c5b2-4542-8765-00480fd6043d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211242
Listing Expiration
2026-12-31
Marketing Start
2020-12-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72078002
Hyphenated Format
72078-002
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
norepinephrine bitartrate (source: ndc)
Generic Name
norepinephrine bitartrate (source: ndc)
Application Number
ANDA211242 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (72078-002-04) / 4 mL in 1 VIAL, SINGLE-DOSE (72078-002-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f55bd465-c5b2-4542-8765-00480fd6043d", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["7a4950ea-6369-4dd5-97be-df21a5a5055f"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (72078-002-04) / 4 mL in 1 VIAL, SINGLE-DOSE (72078-002-00)", "package_ndc": "72078-002-04", "marketing_start_date": "20201204"}], "brand_name": "Norepinephrine bitartrate", "product_id": "72078-002_f55bd465-c5b2-4542-8765-00480fd6043d", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "72078-002", "generic_name": "Norepinephrine bitartrate", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norepinephrine bitartrate", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA211242", "marketing_category": "ANDA", "marketing_start_date": "20201204", "listing_expiration_date": "20261231"}