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Spironolactone - 63739-544-10 - (Spironolactone)

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Drug Information of Spironolactone

Product NDC: 63739-544
Proprietary Name: Spironolactone
Non Proprietary Name: Spironolactone
Active Ingredient(s): 25    mg/1 & nbsp;   Spironolactone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Spironolactone

Product NDC: 63739-544
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091426
Marketing Category: ANDA
Start Marketing Date: 20110601

Package Information of Spironolactone

Package NDC: 63739-544-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-544-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Spironolactone

NDC Code 63739-544-10
Proprietary Name Spironolactone
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-544-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-544
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
Substance Name SPIRONOLACTONE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

Complete Information of Spironolactone


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