heparin sodium in sodium chloride

Generic: heparin sodium

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name heparin sodium in sodium chloride
Generic Name heparin sodium
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

heparin sodium 200 [USP'U]/100mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-0428
Product ID 0338-0428_68b37381-6db4-4ac0-ba6b-3204add02665
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018609
Listing Expiration 2026-12-31
Marketing Start 1982-04-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03380428
Hyphenated Format 0338-0428

Supplemental Identifiers

RxCUI
1658690 1658692
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 in sodium chloride (source: ndc)
Generic Name heparin sodium (source: ndc)
Application Number NDA018609 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 [USP'U]/100mL
source: ndc
Packaging
  • 12 BAG in 1 CARTON (0338-0428-12) / 1000 mL in 1 BAG
source: ndc

Packages (1)

0338-0428-12 12 BAG in 1 CARTON (0338-0428-12) / 1000 mL in 1 BAG

Ingredients (1)

heparin sodium (200 [USP'U]/100mL)

Linked Drug Pages (1)

HEPARIN SODIUM IN SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "68b37381-6db4-4ac0-ba6b-3204add02665", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658690", "1658692"], "spl_set_id": ["0d929726-76c3-48fc-b4e7-fd06409f9fb3"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BAG in 1 CARTON (0338-0428-12)  / 1000 mL in 1 BAG", "package_ndc": "0338-0428-12", "marketing_start_date": "20200423"}], "brand_name": "HEPARIN SODIUM IN SODIUM CHLORIDE", "product_id": "0338-0428_68b37381-6db4-4ac0-ba6b-3204add02665", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0338-0428", "generic_name": "HEPARIN SODIUM", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HEPARIN SODIUM IN SODIUM CHLORIDE", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "200 [USP'U]/100mL"}], "application_number": "NDA018609", "marketing_category": "NDA", "marketing_start_date": "19820428", "listing_expiration_date": "20261231"}