NDC 55292-702

Panhematin

Hemin

Panhematin is a Intravenous Powder, For Solution in the Human Prescription Drug category. It is labeled and distributed by Recordati Rare Diseases, Inc.. The primary component is Hemin.

• Product ID: 55292-702_997ac971-218e-4936-a26c-807f3c4d8f3a
• NDC: 55292-702
• Product Type: Human Prescription Drug
• Proprietary Name: Panhematin
• Generic Name: Hemin
• Dosage Form: Powder, For Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 1983-07-20
• Marketing Category: BLA / BLA
• Application Number: BLA101246
• Labeler Name: RECORDATI RARE DISEASES, INC.
• Substance Name: HEMIN
• Active Ingredient Strength: 7 mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 55292-702-55

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

• Marketing Start Date: 1983-07-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55292-702-55 [55292070255]

Panhematin POWDER, FOR SOLUTION

• Marketing Category: BLA
• Application Number: BLA101246
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1983-07-20

NDC 55292-702-54 [55292070254]

Panhematin POWDER, FOR SOLUTION

• Marketing Category: BLA
• Application Number: BLA101246
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1983-07-20

Drug Details

Active Ingredients

Ingredient	Strength
HEMIN	7 mg/mL

OpenFDA Data

• SPL SET ID: 9984267a-4d57-4444-9bb5-16bca7dea691
• Manufacturer:
  • RECORDATI RARE DISEASES, INC.
• UNII:
  • 743LRP9S7N
• RxNorm Concept Unique ID - RxCUI:
  • 1926454
  • 1926452

NDC Crossover Matching brand name "Panhematin" or generic name "Hemin"

NDC	Brand Name	Generic Name
55292-701	Panhematin	hemin
55292-702	Panhematin	hemin