NDC 59630-551

Mulpleta

Lusutrombopag

Mulpleta is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Shionogi Inc.. The primary component is Lusutrombopag.

• Product ID: 59630-551_26dfeb62-c27f-4b13-bf37-6c9a36c20c33
• NDC: 59630-551
• Product Type: Human Prescription Drug
• Proprietary Name: Mulpleta
• Generic Name: Lusutrombopag
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2018-08-27
• Marketing Category: NDA / NDA
• Application Number: NDA210923
• Labeler Name: SHIONOGI INC.
• Substance Name: LUSUTROMBOPAG
• Active Ingredient Strength: 3 mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 59630-551-07

1 DOSE PACK in 1 CARTON (59630-551-07) > 7 TABLET, FILM COATED in 1 DOSE PACK

• Marketing Start Date: 2018-08-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59630-551-07 [59630055107]

Mulpleta TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA210923
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-08-27

Drug Details

Active Ingredients

Ingredient	Strength
LUSUTROMBOPAG	3 mg/1

OpenFDA Data

• SPL SET ID: f9fd0cfd-717d-4a87-99bc-de7b38807e55
• Manufacturer:
  • SHIONOGI INC.
• UNII:
  • 6LL5JFU42F
• RxNorm Concept Unique ID - RxCUI:
  • 2054989
  • 2054995