Package 71839-118-25

Brand: heparin sodium

Generic: heparin sodium
NDC Package

Package Facts

Identity

Package NDC 71839-118-25
Digits Only 7183911825
Product NDC 71839-118
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (71839-118-25) / .5 mL in 1 VIAL, SINGLE-DOSE (71839-118-01)

Marketing

Marketing Status
Marketed Since 2020-12-29
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": "8d799a63-ec08-466c-9bba-cd4a1eebc698", "openfda": {"upc": ["0371839118014"], "unii": ["ZZ45AB24CA"], "rxcui": ["1658634"], "spl_set_id": ["6be171fb-c85f-4336-a88d-b4d97bb0fe03"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71839-118-25)  / .5 mL in 1 VIAL, SINGLE-DOSE (71839-118-01)", "package_ndc": "71839-118-25", "marketing_start_date": "20201229"}], "brand_name": "Heparin Sodium", "product_id": "71839-118_8d799a63-ec08-466c-9bba-cd4a1eebc698", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "71839-118", "generic_name": "Heparin Sodium", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "5000 [USP'U]/.5mL"}], "application_number": "ANDA214839", "marketing_category": "ANDA", "marketing_start_date": "20201229", "listing_expiration_date": "20261231"}