Package 0338-9669-01

Brand: anticoagulant sodium citrate

Generic: trisodium citrate dihydrate
NDC Package

Package Facts

Identity

Package NDC 0338-9669-01
Digits Only 0338966901
Product NDC 0338-9669
Product ID 0338-9669_8855e600-2002-4c8b-94dc-d275de33169b
Description

250 mL in 1 BAG (0338-9669-01)

Marketing

Marketing Status
Marketed Since 2024-04-02
Brand anticoagulant sodium citrate
Generic trisodium citrate dihydrate
Sample Package No

Linked Drug Pages (1)

ANTICOAGULANT SODIUM CITRATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EXTRACORPOREAL"], "spl_id": "8855e600-2002-4c8b-94dc-d275de33169b", "openfda": {"unii": ["B22547B95K"], "spl_set_id": ["7025a0f9-1a56-4416-a3a4-925d755aed90"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (0338-9669-01)", "package_ndc": "0338-9669-01", "marketing_start_date": "20240402"}], "brand_name": "ANTICOAGULANT SODIUM CITRATE", "product_id": "0338-9669_8855e600-2002-4c8b-94dc-d275de33169b", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "0338-9669", "generic_name": "trisodium citrate dihydrate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ANTICOAGULANT SODIUM CITRATE", "active_ingredients": [{"name": "TRISODIUM CITRATE DIHYDRATE", "strength": "40 mg/mL"}], "application_number": "BN980123", "marketing_category": "NDA", "marketing_start_date": "20240402", "listing_expiration_date": "20271231"}