RIMSO-50

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 790384502

Effective Date

March 17, 2021

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

67457-177

Application Number

NDA017788

Marketing Category

NDA (C73594)

Route of Administration

INTRAVESICAL

Effective Date

October 18, 2017

Ingredients

WATERInactive

Code: 059QF0KO0RClass: IACT

Code: YOW8V9698HClass: ACTIBQuantity: 0.54 g in 1 mL