Furosemide

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Labeler

A-S Medication Solutions

DUNS Number

830016429

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

NDC Product Code

50090-6219

Application Number

NDA018823

Marketing Category

NDA (C73594)

Route of Administration

ORAL

Effective Date

July 14, 2017

Ingredients

Code: 7LXU5N7ZO5Class: ACTIBQuantity: 20 mg in 1 1

SILICON DIOXIDEInactive

Code: ETJ7Z6XBU4Class: IACT

SODIUM LAURYL SULFATEInactive

Code: 368GB5141JClass: IACT

LACTOSE MONOHYDRATEInactive

Code: EWQ57Q8I5XClass: IACT

MICROCRYSTALLINE CELLULOSEInactive

Code: OP1R32D61UClass: IACT

STARCH, CORNInactive

Code: O8232NY3SJClass: IACT

SODIUM STARCH GLYCOLATE TYPE A POTATOInactive

Code: 5856J3G2A2Class: IACT

STEARIC ACIDInactive

Code: 4ELV7Z65APClass: IACT