heparin sodium
Generic: heparin sodium
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
heparin sodium 10000 [USP'U]/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1411
Product ID
51662-1411_0fcb6a01-0cd9-a1df-e063-6394a90abb78
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018916
Listing Expiration
2026-12-31
Marketing Start
2019-11-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621411
Hyphenated Format
51662-1411
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
heparin sodium (source: ndc)
Generic Name
heparin sodium (source: ndc)
Application Number
NDA018916 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10000 [USP'U]/100mL
Packaging
- 24 POUCH in 1 CASE (51662-1411-3) / 1 POUCH in 1 POUCH (51662-1411-2) / 1 BAG in 1 POUCH (51662-1411-1) / 250 mL in 1 BAG
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0fcb6a01-0cd9-a1df-e063-6394a90abb78", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658717"], "spl_set_id": ["97183edd-fa5c-8ff1-e053-2995a90ae1d5"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (51662-1411-3) / 1 POUCH in 1 POUCH (51662-1411-2) / 1 BAG in 1 POUCH (51662-1411-1) / 250 mL in 1 BAG", "package_ndc": "51662-1411-3", "marketing_start_date": "20230922"}], "brand_name": "HEPARIN SODIUM", "product_id": "51662-1411_0fcb6a01-0cd9-a1df-e063-6394a90abb78", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "51662-1411", "generic_name": "HEPARIN SODIUM", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HEPARIN SODIUM", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "10000 [USP'U]/100mL"}], "application_number": "NDA018916", "marketing_category": "NDA", "marketing_start_date": "20191111", "listing_expiration_date": "20261231"}