norepinephrine bitartrate
Generic: norepinephrine bitartrate
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
norepinephrine bitartrate
Generic Name
norepinephrine bitartrate
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION
Routes
Active Ingredients
norepinephrine bitartrate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1528
Product ID
51662-1528_0ff8ef97-006a-e6ca-e063-6294a90a2365
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203662
Listing Expiration
2026-12-31
Marketing Start
2021-08-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621528
Hyphenated Format
51662-1528
Supplemental Identifiers
RxCUI
UNII
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
ANDA203662 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 4 mL in 1 VIAL (51662-1528-1)
- 10 POUCH in 1 CASE (51662-1528-3) / 1 VIAL in 1 POUCH (51662-1528-2) / 4 mL in 1 VIAL
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0ff8ef97-006a-e6ca-e063-6294a90a2365", "openfda": {"unii": ["IFY5PE3ZRW"], "rxcui": ["242969"], "spl_set_id": ["c90d875c-8e6e-284e-e053-2a95a90a334f"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "4 mL in 1 VIAL (51662-1528-1)", "package_ndc": "51662-1528-1", "marketing_start_date": "20210808"}, {"sample": false, "description": "10 POUCH in 1 CASE (51662-1528-3) / 1 VIAL in 1 POUCH (51662-1528-2) / 4 mL in 1 VIAL", "package_ndc": "51662-1528-3", "marketing_start_date": "20220710"}], "brand_name": "NOREPINEPHRINE BITARTRATE", "product_id": "51662-1528_0ff8ef97-006a-e6ca-e063-6294a90a2365", "dosage_form": "INJECTION", "pharm_class": ["Catecholamine [EPC]", "Catecholamines [CS]"], "product_ndc": "51662-1528", "generic_name": "NOREPINEPHRINE BITARTRATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NOREPINEPHRINE BITARTRATE", "active_ingredients": [{"name": "NOREPINEPHRINE BITARTRATE", "strength": "1 mg/mL"}], "application_number": "ANDA203662", "marketing_category": "ANDA", "marketing_start_date": "20210808", "listing_expiration_date": "20261231"}