norepinephrine bitartrate
Generic: norepinephrine bitartrate
Labeler: camber pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
norepinephrine bitartrate
Generic Name
norepinephrine bitartrate
Labeler
camber pharmaceuticals, inc.
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
norepinephrine bitartrate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
31722-372
Product ID
31722-372_375cf9eb-4989-ae9e-e063-6394a90a39a9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA219163
Listing Expiration
2026-12-31
Marketing Start
2025-01-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
31722372
Hyphenated Format
31722-372
Supplemental Identifiers
RxCUI
UPC
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
ANDA219163 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (31722-372-32) / 4 mL in 1 VIAL, SINGLE-DOSE (31722-372-31)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "375cf9eb-4989-ae9e-e063-6394a90a39a9", "openfda": {"upc": ["0331722372312"], "unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["baba1002-8b62-4a24-a4e1-53e7a59c785a"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (31722-372-32) / 4 mL in 1 VIAL, SINGLE-DOSE (31722-372-31)", "package_ndc": "31722-372-32", "marketing_start_date": "20250131"}], "brand_name": "Norepinephrine bitartrate", "product_id": "31722-372_375cf9eb-4989-ae9e-e063-6394a90a39a9", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "31722-372", "generic_name": "Norepinephrine bitartrate", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norepinephrine bitartrate", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA219163", "marketing_category": "ANDA", "marketing_start_date": "20250131", "listing_expiration_date": "20261231"}