heparin sodium
Generic: heparin sodium
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
heparin sodium
Generic Name
heparin sodium
Labeler
remedyrepack inc.
Dosage Form
INJECTION
Routes
Active Ingredients
heparin sodium 5000 [USP'U]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4547
Product ID
70518-4547_4885975b-67c0-5519-e063-6394a90a105b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017037
Listing Expiration
2027-12-31
Marketing Start
2026-01-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184547
Hyphenated Format
70518-4547
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
NDA017037 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5000 [USP'U]/mL
Packaging
- 25 VIAL in 1 PACKAGE (70518-4547-0) / 1 mL in 1 VIAL (70518-4547-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "4885975b-67c0-5519-e063-6394a90a105b", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1659263"], "spl_set_id": ["a5fab0b1-c472-489c-ba87-2f8e53356173"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 PACKAGE (70518-4547-0) / 1 mL in 1 VIAL (70518-4547-1)", "package_ndc": "70518-4547-0", "marketing_start_date": "20260116"}], "brand_name": "Heparin Sodium", "product_id": "70518-4547_4885975b-67c0-5519-e063-6394a90a105b", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "70518-4547", "generic_name": "Heparin Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "NDA017037", "marketing_category": "NDA", "marketing_start_date": "20260116", "listing_expiration_date": "20271231"}