Package 55292-702-55

Brand: panhematin

Generic: hemin
NDC Package

Package Facts

Identity

Package NDC 55292-702-55
Digits Only 5529270255
Product NDC 55292-702
Description

1 VIAL in 1 CARTON (55292-702-55) / 48 mL in 1 VIAL (55292-702-54)

Marketing

Marketing Status
Marketed Since 1983-07-20
Brand panhematin
Generic hemin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ff0139fe-eb46-4d22-95f1-849de7ce9462", "openfda": {"unii": ["743LRP9S7N"], "rxcui": ["1926452", "1926454"], "spl_set_id": ["9984267a-4d57-4444-9bb5-16bca7dea691"], "manufacturer_name": ["Recordati Rare Diseases, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (55292-702-55)  / 48 mL in 1 VIAL (55292-702-54)", "package_ndc": "55292-702-55", "marketing_start_date": "19830720"}], "brand_name": "Panhematin", "product_id": "55292-702_ff0139fe-eb46-4d22-95f1-849de7ce9462", "dosage_form": "POWDER, FOR SOLUTION", "product_ndc": "55292-702", "generic_name": "hemin", "labeler_name": "Recordati Rare Diseases, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Panhematin", "active_ingredients": [{"name": "HEMIN", "strength": "7 mg/mL"}], "application_number": "BLA101246", "marketing_category": "BLA", "marketing_start_date": "19830720", "listing_expiration_date": "20271231"}