NDC 44087-8822

Rebif

Interferon Beta-1a

Rebif is a Subcutaneous Kit in the Human Prescription Drug category. It is labeled and distributed by Emd Serono, Inc.. The primary component is .

• Product ID: 44087-8822_0b175df7-7507-4d2f-bddf-65f707392420
• NDC: 44087-8822
• Product Type: Human Prescription Drug
• Proprietary Name: Rebif
• Generic Name: Interferon Beta-1a
• Dosage Form: Kit
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 2004-12-17
• Marketing Category: BLA / BLA
• Application Number: BLA103780
• Labeler Name: EMD Serono, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 44087-8822-1

1 KIT in 1 CARTON (44087-8822-1) * .2 mL in 1 SYRINGE, GLASS * .5 mL in 1 SYRINGE, GLASS

• Marketing Start Date: 2004-12-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44087-8822-1 [44087882201]

Rebif KIT

• Marketing Category: BLA
• Application Number: BLA103780
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2004-12-17

Drug Details

OpenFDA Data

• SPL SET ID: c6fcb5d2-8fcd-44fa-a838-b84ee5f44f0f
• Manufacturer:
  • EMD Serono, Inc.
• UNII:
  • XRO4566Q4R
• RxNorm Concept Unique ID - RxCUI:
  • 758028
  • 758029
  • 795748
  • 795749
  • 1650268
  • 1650282
  • 758025
  • 758027
  • 758032
  • 758030
  • 1650012
  • 1650004
  • 1650011
  • 1649994
  • 1650003
  • 1649996

NDC Crossover Matching brand name "Rebif" or generic name "Interferon Beta-1a"

NDC	Brand Name	Generic Name
44087-0022	REBIF	INTERFERON BETA-1A
44087-0044	REBIF	interferon beta-1a
44087-8822	Rebif	interferon beta-1a
59627-002	Avonex	Interferon Beta-1a
44087-0188	REBIF REBIDOSE	INTERFERON BETA-1A
44087-3322	REBIF REBIDOSE	INTERFERON BETA-1A
44087-3344	REBIF REBIDOSE	INTERFERON BETA-1A