Package 71288-400-03
Brand: heparin sodium
Generic: heparin sodiumPackage Facts
Identity
Package NDC
71288-400-03
Digits Only
7128840003
Product NDC
71288-400
Description
25 VIAL, SINGLE-DOSE in 1 CARTON (71288-400-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-400-02)
Marketing
Marketing Status
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": "dabdb746-a0fb-4208-ab3c-32e638396713", "openfda": {"unii": ["ZZ45AB24CA"], "rxcui": ["1658647"], "spl_set_id": ["83a59e7d-63e9-4eb8-87f0-52039d6893a5"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71288-400-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-400-02)", "package_ndc": "71288-400-03", "marketing_start_date": "20190615"}], "brand_name": "Heparin Sodium", "product_id": "71288-400_dabdb746-a0fb-4208-ab3c-32e638396713", "dosage_form": "INJECTION", "pharm_class": ["Anti-coagulant [EPC]", "Heparin [CS]", "Unfractionated Heparin [EPC]"], "product_ndc": "71288-400", "generic_name": "Heparin Sodium", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Heparin Sodium", "active_ingredients": [{"name": "HEPARIN SODIUM", "strength": "2000 [USP'U]/2mL"}], "application_number": "ANDA211005", "marketing_category": "ANDA", "marketing_start_date": "20190615", "listing_expiration_date": "20261231"}