Furosemide - 0603-3739-34 - (furosemide)

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Drug Information of Furosemide

Product NDC: 0603-3739
Proprietary Name: Furosemide
Non Proprietary Name: furosemide
Active Ingredient(s): 20    mg/1 & nbsp;   furosemide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Furosemide

Product NDC: 0603-3739
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076796
Marketing Category: ANDA
Start Marketing Date: 20040326

Package Information of Furosemide

Package NDC: 0603-3739-34
Package Description: 5000 TABLET in 1 BOTTLE, PLASTIC (0603-3739-34)

NDC Information of Furosemide

NDC Code 0603-3739-34
Proprietary Name Furosemide
Package Description 5000 TABLET in 1 BOTTLE, PLASTIC (0603-3739-34)
Product NDC 0603-3739
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name furosemide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040326
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name FUROSEMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]

Complete Information of Furosemide


General Information