Package 87081-467-91

Brand: desferal

Generic: deferoxamine mesylate
NDC Package

Package Facts

Identity

Package NDC 87081-467-91
Digits Only 8708146791
Product NDC 87081-467
Description

4 mL in 1 VIAL (87081-467-91)

Marketing

Marketing Status
Marketed Since 1968-04-02
Brand desferal
Generic deferoxamine mesylate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "38eff751-96c6-c48a-e063-6294a90a0e48", "openfda": {"unii": ["V9TKO7EO6K"], "rxcui": ["1731350", "1731352"], "spl_set_id": ["38eff751-96c5-c48a-e063-6294a90a0e48"], "manufacturer_name": ["MITEM PHARMA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 mL in 1 VIAL (87081-467-91)", "package_ndc": "87081-467-91", "marketing_start_date": "19680402"}], "brand_name": "Desferal", "product_id": "87081-467_38eff751-96c6-c48a-e063-6294a90a0e48", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "87081-467", "generic_name": "deferoxamine mesylate", "labeler_name": "MITEM PHARMA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desferal", "active_ingredients": [{"name": "DEFEROXAMINE MESYLATE", "strength": "500 mg/5mL"}], "application_number": "NDA016267", "marketing_category": "NDA", "marketing_start_date": "19680402", "listing_expiration_date": "20261231"}