norepinephrine bitartrate
Generic: norepinephrine bitartrate
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
norepinephrine bitartrate
Generic Name
norepinephrine bitartrate
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
norepinephrine bitartrate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-316
Product ID
25021-316_61b38873-cf8d-48b6-b126-2e0a32ac5f7a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214323
Listing Expiration
2026-12-31
Marketing Start
2021-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021316
Hyphenated Format
25021-316
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
ANDA214323 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL in 1 CARTON (25021-316-04) / 4 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "61b38873-cf8d-48b6-b126-2e0a32ac5f7a", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["cc9ecec5-3bd7-4132-9745-7666bac8ceac"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-316-04) / 4 mL in 1 VIAL", "package_ndc": "25021-316-04", "marketing_start_date": "20210701"}], "brand_name": "Norepinephrine Bitartrate", "product_id": "25021-316_61b38873-cf8d-48b6-b126-2e0a32ac5f7a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "25021-316", "generic_name": "Norepinephrine Bitartrate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norepinephrine Bitartrate", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA214323", "marketing_category": "ANDA", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}