Furosemide - 0409-1639-10 - (FUROSEMIDE)

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Drug Information of Furosemide

Product NDC: 0409-1639
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: 0409-1639
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075241
Marketing Category: ANDA
Start Marketing Date: 19990528

Package Information of Furosemide

Package NDC: 0409-1639-10
Package Description: 10 CARTON in 1 CONTAINER (0409-1639-10) > 1 SYRINGE, PLASTIC in 1 CARTON > 10 mL in 1 SYRINGE, PLASTIC

NDC Information of Furosemide

NDC Code 0409-1639-10
Proprietary Name Furosemide
Package Description 10 CARTON in 1 CONTAINER (0409-1639-10) > 1 SYRINGE, PLASTIC in 1 CARTON > 10 mL in 1 SYRINGE, PLASTIC
Product NDC 0409-1639
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FUROSEMIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19990528
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
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