NDC 55292-701

Panhematin

Hemin

Panhematin is a Intravenous Injection, Powder, Lyophilized, 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: 55292-701_cdfd9947-bc51-43c9-9bd0-130c214bb68a
• NDC: 55292-701
• Product Type: Human Prescription Drug
• Proprietary Name: Panhematin
• Generic Name: Hemin
• Dosage Form: Injection, Powder, Lyophilized, For Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 1983-07-20
• Marketing End Date: 2020-01-24
• 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

Packaging

NDC 55292-701-55

1 VIAL in 1 CARTON (55292-701-55) > 43 mL in 1 VIAL (55292-701-54)

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

NDC SPL Data Element Entries

NDC 55292-701-55 [55292070155]

Panhematin INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: BLA
• Application Number: BLA101246
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1983-07-20
• Marketing End Date: 2020-01-24

NDC 55292-701-54 [55292070154]

Panhematin INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

• Marketing Category: BLA
• Application Number: BLA101246
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1983-07-20
• Marketing End Date: 2020-01-24

Drug Details

Active Ingredients

Ingredient	Strength
HEMIN	7 mg/mL

OpenFDA Data

• SPL SET ID: d84808a8-d039-6293-6e0d-782327f0a5c0
• Manufacturer:
  • RECORDATI RARE DISEASES, INC.
• UNII:
  • 743LRP9S7N
• RxNorm Concept Unique ID - RxCUI:
  • 213400
  • 238657
• UPC Code:
  • 0367386701540

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

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