panhematin

Generic: hemin

Labeler: recordati rare diseases, inc.
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name panhematin
Generic Name hemin
Labeler recordati rare diseases, inc.
Dosage Form POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

hemin 7 mg/mL

Manufacturer
Recordati Rare Diseases, Inc.

Identifiers & Regulatory

Product NDC 55292-702
Product ID 55292-702_ff0139fe-eb46-4d22-95f1-849de7ce9462
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA101246
Listing Expiration 2027-12-31
Marketing Start 1983-07-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55292702
Hyphenated Format 55292-702

Supplemental Identifiers

RxCUI
1926452 1926454
UNII
743LRP9S7N

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name panhematin (source: ndc)
Generic Name hemin (source: ndc)
Application Number BLA101246 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 7 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (55292-702-55) / 48 mL in 1 VIAL (55292-702-54)
source: ndc

Packages (1)

Ingredients (1)

hemin (7 mg/mL)

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"}