NDC 54746-001

Alferon

Interferon Alfa-n3

Alferon is a Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by Hemispherx Biopharma, Inc. The primary component is Interferon Alfa-n3.

• Product ID: 54746-001_77546126-9b82-08bd-e053-2991aa0a3b3d
• NDC: 54746-001
• Product Type: Human Prescription Drug
• Proprietary Name: Alferon
• Generic Name: Interferon Alfa-n3
• Dosage Form: Injection
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 1989-10-10
• Marketing Category: BLA / BLA
• Application Number: BLA103158
• Labeler Name: Hemispherx Biopharma, Inc
• Substance Name: INTERFERON ALFA-N3
• Active Ingredient Strength: 5000000 [arb'U]/mL
• Pharm Classes: Interferon alpha [EPC],Interferon-alpha [Chemical/Ingredient]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 54746-001-01

0 mL in 1 VIAL, GLASS (54746-001-01)

• Marketing Start Date: 1989-10-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54746-001-01 [54746000101]

Alferon INJECTION

• Marketing Category: BLA
• Application Number: BLA103158
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 1989-10-10

Drug Details

Active Ingredients

Ingredient	Strength
INTERFERON ALFA-N3	5000000 [arb'U]/mL

OpenFDA Data

• SPL SET ID: 241ece31-e649-021a-e054-00144ff8d46c
• Manufacturer:
  • Hemispherx Biopharma, Inc
• UNII:
  • 47BPR3V3MP
• RxNorm Concept Unique ID - RxCUI:
  • 598014
  • 615136

Pharmacological Class

• Interferon alpha [EPC]
• Interferon-alpha [Chemical/Ingredient]