Package 81565-203-02

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 81565-203-02
Digits Only 8156520302
Product NDC 81565-203
Description

25 VIAL in 1 TRAY (81565-203-02) / 10 mL in 1 VIAL (81565-203-01)

Marketing

Marketing Status
Marketed Since 2022-03-07
Brand heparin sodium
Generic heparin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "4bebb181-0ed2-44b0-af0d-4802862e73b4", "openfda": {"upc": ["0381565203014"], "unii": ["ZZ45AB24CA"], "rxcui": ["1361226"], "spl_set_id": ["cece935c-1c0a-4949-b023-d6df3d53fbfa"], "manufacturer_name": ["Phlow Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (81565-203-02)  / 10 mL in 1 VIAL (81565-203-01)", "package_ndc": "81565-203-02", "marketing_start_date": "20220307"}], "brand_name": "Heparin Sodium", "product_id": "81565-203_4bebb181-0ed2-44b0-af0d-4802862e73b4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "81565-203", "generic_name": "HEPARIN SODIUM", "labeler_name": "Phlow Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "1000 [USP'U]/mL"}], "application_number": "NDA017029", "marketing_category": "NDA", "marketing_start_date": "20220307", "listing_expiration_date": "20261231"}