heparin sodium

Generic: heparin sodium

Labeler: pfizer laboratories div pfizer inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium
Generic Name heparin sodium
Labeler pfizer laboratories div pfizer inc
Dosage Form INJECTION
Routes
INTRAVENOUS SUBCUTANEOUS
Active Ingredients

heparin sodium 1000 [USP'U]/mL

Manufacturer
Pfizer Laboratories Div Pfizer Inc

Identifiers & Regulatory

Product NDC 0069-0043
Product ID 0069-0043_4ba8e8f9-4192-46ea-96b0-6a2e45547581
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA201370
Listing Expiration 2026-12-31
Marketing Start 2011-07-21

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00690043
Hyphenated Format 0069-0043

Supplemental Identifiers

RxCUI
1361226 1361615 1362831 1658647
UPC
0300690058016
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 NDA201370 (source: ndc)
Routes
INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1000 [USP'U]/mL
source: ndc
Packaging
  • 25 VIAL in 1 CONTAINER (0069-0043-01) / 2 mL in 1 VIAL (0069-0043-02)
source: ndc

Packages (1)

0069-0043-01 25 VIAL in 1 CONTAINER (0069-0043-01) / 2 mL in 1 VIAL (0069-0043-02)

Ingredients (1)

heparin sodium (1000 [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": "4ba8e8f9-4192-46ea-96b0-6a2e45547581", "openfda": {"upc": ["0300690058016"], "unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615", "1362831", "1658647"], "spl_set_id": ["56dc3074-f1c5-45a3-b923-f1d14858e06d"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CONTAINER (0069-0043-01)  / 2 mL in 1 VIAL (0069-0043-02)", "package_ndc": "0069-0043-01", "marketing_start_date": "20110721"}], "brand_name": "Heparin Sodium", "product_id": "0069-0043_4ba8e8f9-4192-46ea-96b0-6a2e45547581", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0069-0043", "generic_name": "Heparin Sodium", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "NDA201370", "marketing_category": "NDA", "marketing_start_date": "20110721", "listing_expiration_date": "20261231"}