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Spironolactone - 43063-072-01 - (Spironolactone)

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Drug Information of Spironolactone

Product NDC: 43063-072
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: 43063-072
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091426
Marketing Category: ANDA
Start Marketing Date: 20100802

Package Information of Spironolactone

Package NDC: 43063-072-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (43063-072-01)

NDC Information of Spironolactone

NDC Code 43063-072-01
Proprietary Name Spironolactone
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (43063-072-01)
Product NDC 43063-072
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100802
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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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