Package 0338-0431-03
Brand: heparin sodium in sodium chloride
Generic: heparin sodiumPackage Facts
Identity
Package NDC
0338-0431-03
Digits Only
0338043103
Product NDC
0338-0431
Description
18 BAG in 1 CARTON (0338-0431-03) / 500 mL in 1 BAG
Marketing
Marketing Status
Brand
heparin sodium in sodium chloride
Generic
heparin sodium
Sample Package
No
Linked Drug Pages (1)
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": "18 BAG in 1 CARTON (0338-0431-03) / 500 mL in 1 BAG", "package_ndc": "0338-0431-03", "marketing_start_date": "19820428"}], "brand_name": "HEPARIN SODIUM IN SODIUM CHLORIDE", "product_id": "0338-0431_68b37381-6db4-4ac0-ba6b-3204add02665", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "0338-0431", "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"}