norepinephrine bitartrate

Generic: norepinephrine bitartrate

Labeler: be pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name norepinephrine bitartrate
Generic Name norepinephrine bitartrate
Labeler be pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

norepinephrine bitartrate 1 mg/mL

Manufacturer
BE Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71839-143
Product ID 71839-143_c42d425a-094e-4390-b4f9-4bb4b0fbc7d0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217575
Listing Expiration 2026-12-31
Marketing Start 2023-12-30

Pharmacologic Class

Classes
catecholamine [epc] catecholamines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71839143
Hyphenated Format 71839-143

Supplemental Identifiers

RxCUI
242969
UPC
0371839143252 0371839143016 0371839143108
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 ANDA217575 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (71839-143-10) / 4 mL in 1 VIAL, SINGLE-DOSE (71839-143-01)
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (71839-143-25) / 4 mL in 1 VIAL, SINGLE-DOSE (71839-143-01)
source: ndc

Packages (2)

71839-143-10 10 VIAL, SINGLE-DOSE in 1 CARTON (71839-143-10) / 4 mL in 1 VIAL, SINGLE-DOSE (71839-143-01) 71839-143-25 25 VIAL, SINGLE-DOSE in 1 CARTON (71839-143-25) / 4 mL in 1 VIAL, SINGLE-DOSE (71839-143-01)

Ingredients (1)

norepinephrine bitartrate (1 mg/mL)

Linked Drug Pages (1)

Norepinephrine Bitartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c42d425a-094e-4390-b4f9-4bb4b0fbc7d0", "openfda": {"upc": ["0371839143252", "0371839143016", "0371839143108"], "unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["c42d425a-094e-4390-b4f9-4bb4b0fbc7d0"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (71839-143-10)  / 4 mL in 1 VIAL, SINGLE-DOSE (71839-143-01)", "package_ndc": "71839-143-10", "marketing_start_date": "20231230"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71839-143-25)  / 4 mL in 1 VIAL, SINGLE-DOSE (71839-143-01)", "package_ndc": "71839-143-25", "marketing_start_date": "20231230"}], "brand_name": "Norepinephrine Bitartrate", "product_id": "71839-143_c42d425a-094e-4390-b4f9-4bb4b0fbc7d0", "dosage_form": "INJECTION", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "71839-143", "generic_name": "norepinephrine bitartrate", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norepinephrine Bitartrate", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA217575", "marketing_category": "ANDA", "marketing_start_date": "20231230", "listing_expiration_date": "20261231"}