Package 25021-402-66

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 25021-402-66
Digits Only 2502140266
Product NDC 25021-402
Description

25 VIAL in 1 CARTON (25021-402-66) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2014-07-01
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": "b44c59b9-34b9-4244-90a8-928c20ad1e84", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615", "1362831"], "spl_set_id": ["ef309d83-7262-4874-8580-f4ca254f963a"], "manufacturer_name": ["Sagent Pharmaceticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-402-66)  / 1 mL in 1 VIAL", "package_ndc": "25021-402-66", "marketing_start_date": "20140701"}], "brand_name": "Heparin Sodium", "product_id": "25021-402_b44c59b9-34b9-4244-90a8-928c20ad1e84", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "25021-402", "generic_name": "Heparin Sodium", "labeler_name": "Sagent Pharmaceticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "ANDA090808", "marketing_category": "ANDA", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}