norepinephrine bitartrate

Generic: norepinephrine bitartrate

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name norepinephrine bitartrate
Generic Name norepinephrine bitartrate
Labeler baxter healthcare corporation
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

norepinephrine bitartrate 1 mg/mL

Manufacturer
Baxter Healthcare Corporation

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
catecholamine [epc] catecholamines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 36000162
Hyphenated Format 36000-162

Supplemental Identifiers

RxCUI
242969
UNII
IFY5PE3ZRW

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 10 AMPULE in 1 CARTON (36000-162-10) / 4 mL in 1 AMPULE (36000-162-01)
source: ndc

Packages (1)

Ingredients (1)

norepinephrine bitartrate (1 mg/mL)

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"}