Package 68083-136-25

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 68083-136-25
Digits Only 6808313625
Product NDC 68083-136
Description

25 VIAL in 1 CARTON (68083-136-25) / 1 mL in 1 VIAL (68083-136-01)

Marketing

Marketing Status
Marketed Since 2017-03-09
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": "794ab494-666a-4e82-ba24-982189a20255", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1361226", "1361615"], "spl_set_id": ["301b19bc-21c2-4a35-9d29-569b08d855c4"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (68083-136-25)  / 1 mL in 1 VIAL (68083-136-01)", "package_ndc": "68083-136-25", "marketing_start_date": "20170309"}], "brand_name": "Heparin Sodium", "product_id": "68083-136_794ab494-666a-4e82-ba24-982189a20255", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "68083-136", "generic_name": "Heparin Sodium", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/mL"}], "application_number": "ANDA205323", "marketing_category": "ANDA", "marketing_start_date": "20170309", "listing_expiration_date": "20261231"}