NDC 44087-9070

Gonal-f

Follitropin Alfa

Gonal-f 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: 44087-9070_1b6255d2-7c87-4f6c-ade6-481959825fb7
• NDC: 44087-9070
• Product Type: Human Prescription Drug
• Proprietary Name: Gonal-f
• Generic Name: Follitropin Alfa
• Dosage Form: Kit
• Route of Administration: SUBCUTANEOUS
• Marketing Start Date: 2004-03-25
• Marketing Category: BLA / NDA
• Application Number: BLA020378
• Labeler Name: EMD Serono, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 44087-9070-1

1 KIT in 1 CARTON (44087-9070-1) * 2 mL in 1 VIAL * 2 mL in 1 SYRINGE

• Marketing Start Date: 2004-03-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44087-9070-1 [44087907001]

Gonal-f KIT

• Marketing Category: BLA
• Application Number: BLA020378
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2004-03-25

Drug Details

OpenFDA Data

• SPL SET ID: ae85b9c3-e7eb-4981-a5d9-346050e8f189
• Manufacturer:
  • EMD Serono, Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 351125
  • 351993

NDC Crossover Matching brand name "Gonal-f" or generic name "Follitropin Alfa"

NDC	Brand Name	Generic Name
44087-9030	Gonal-f	follitropin alfa
44087-9070	Gonal-f	follitropin alfa
44087-9005	GONAL-F RFF	follitropin alfa
50090-6049	GONAL-F RFF	follitropin alfa