norepinephrine bitartrate
Generic: norepinephrine bitartrate
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
norepinephrine bitartrate
Generic Name
norepinephrine bitartrate
Labeler
baxter healthcare corporation
Dosage Form
INJECTION
Routes
Active Ingredients
norepinephrine bitartrate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
36000-162
Product ID
36000-162_73f5f4bb-09e2-4c5f-b482-c960bb957d53
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040859
Listing Expiration
2026-12-31
Marketing Start
2012-04-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
36000162
Hyphenated Format
36000-162
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
ANDA040859 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 AMPULE in 1 CARTON (36000-162-10) / 4 mL in 1 AMPULE (36000-162-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}