Furosemide - 63323-280-02 - (FUROSEMIDE)

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Drug Information of Furosemide

Product NDC: 63323-280
Proprietary Name: Furosemide
Non Proprietary Name: FUROSEMIDE
Active Ingredient(s): 10    mg/mL & nbsp;   FUROSEMIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 63323-280
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018902
Marketing Category: NDA
Start Marketing Date: 20000712

Package Information of Furosemide

Package NDC: 63323-280-02
Package Description: 25 VIAL in 1 TRAY (63323-280-02) > 2 mL in 1 VIAL

NDC Information of Furosemide

NDC Code 63323-280-02
Proprietary Name Furosemide
Package Description 25 VIAL in 1 TRAY (63323-280-02) > 2 mL in 1 VIAL
Product NDC 63323-280
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FUROSEMIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000712
Marketing Category Name NDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name FUROSEMIDE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information