heparin sodium

Generic: heparin sodium

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

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler sandoz inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 5000 [USP'U]/mL

Manufacturer
Sandoz Inc.

Identifiers & Regulatory

Product NDC 0781-3550
Product ID 0781-3550_2ef18b0f-ccc2-5539-e063-6394a90a2a4f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202733
Listing Expiration 2026-12-31
Marketing Start 2014-06-12

Pharmacologic Class

Classes
anti-coagulant [epc] heparin [cs] unfractionated heparin [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07813550
Hyphenated Format 0781-3550

Supplemental Identifiers

RxCUI
1361226 1361574 1361615 1362831 1658647
UPC
0307813545101 0307813439103 0307813555254 0307813541103 0307813543251 0307813541257 0307813543107 0307813550259 0307813439257 0307813533108 0307813555100 0307813550105 0307813540106 0307813538103 0307813540250 0307813533252 0307813538257 0307813545255
UNII
ZZ45AB24CA

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 heparin sodium (source: ndc)
Generic Name heparin sodium (source: ndc)
Application Number ANDA202733 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 5000 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 CARTON (0781-3550-25) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3550-10)
source: ndc

Packages (1)

0781-3550-25 25 VIAL, MULTI-DOSE in 1 CARTON (0781-3550-25) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3550-10)

Ingredients (1)

heparin sodium (5000 [USP'U]/mL)

Linked Drug Pages (1)

Heparin Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2ef18b0f-ccc2-5539-e063-6394a90a2a4f", "openfda": {"upc": ["0307813545101", "0307813439103", "0307813555254", "0307813541103", "0307813543251", "0307813541257", "0307813543107", "0307813550259", "0307813439257", "0307813533108", "0307813555100", "0307813550105", "0307813540106", "0307813538103", "0307813540250", "0307813533252", "0307813538257", "0307813545255"], "unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361574", "1361615", "1362831", "1658647"], "spl_set_id": ["1c634e53-44d6-cdcd-e063-6294a90a92e9"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (0781-3550-25)  / 10 mL in 1 VIAL, MULTI-DOSE (0781-3550-10)", "package_ndc": "0781-3550-25", "marketing_start_date": "20240916"}], "brand_name": "Heparin Sodium", "product_id": "0781-3550_2ef18b0f-ccc2-5539-e063-6394a90a2a4f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0781-3550", "generic_name": "Heparin Sodium", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "ANDA202733", "marketing_category": "ANDA", "marketing_start_date": "20140612", "listing_expiration_date": "20261231"}