NDC 0009-7166

SOMAVERT

Pegvisomant

SOMAVERT is a Kit in the Human Prescription Drug category. It is labeled and distributed by Pharmacia And Upjohn Company Llc. The primary component is .

• Product ID: 0009-7166_3592c83b-dd57-463b-8225-d97905e7ab3d
• NDC: 0009-7166
• Product Type: Human Prescription Drug
• Proprietary Name: SOMAVERT
• Generic Name: Pegvisomant
• Dosage Form: Kit
• Marketing Start Date: 2016-10-01
• Marketing Category: BLA / NDA
• Application Number: BLA021106
• Labeler Name: Pharmacia and Upjohn Company LLC
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0009-7166-01

1 KIT in 1 CARTON (0009-7166-01) * 1 mL in 1 SYRINGE (0009-5936-01) * 1 mL in 1 VIAL, SINGLE-DOSE (0009-5175-02)

• Marketing Start Date: 2016-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0009-7166-01 [00009716601]

SOMAVERT KIT

• Marketing Category: BLA
• Application Number: BLA021106
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-10-01

Drug Details

OpenFDA Data

• SPL SET ID: 3cbb485b-6df1-49ce-8747-592b395b1988
• Manufacturer:
  • Pharmacia and Upjohn Company LLC
• RxNorm Concept Unique ID - RxCUI:
  • 1549452
  • 403807
  • 403806
  • 403808
  • 1549454
  • 1549456
  • 404459
  • 404458
  • 1549323
  • 404457

NDC Crossover Matching brand name "SOMAVERT" or generic name "Pegvisomant"

NDC	Brand Name	Generic Name
0009-5176	SOMAVERT	pegvisomant
0009-5178	SOMAVERT	pegvisomant
0009-5180	SOMAVERT	pegvisomant
0009-5199	SOMAVERT	pegvisomant
0009-5200	SOMAVERT	pegvisomant
0009-7166	SOMAVERT	pegvisomant
0009-7168	SOMAVERT	pegvisomant
0009-7188	SOMAVERT	pegvisomant
0009-7199	SOMAVERT	pegvisomant
0009-7200	SOMAVERT	pegvisomant