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Spironolactone - 68788-9729-6 - (Spironolactone)

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Drug Information of Spironolactone

Product NDC: 68788-9729
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: 68788-9729
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091426
Marketing Category: ANDA
Start Marketing Date: 20121031

Package Information of Spironolactone

Package NDC: 68788-9729-6
Package Description: 60 TABLET in 1 BOTTLE (68788-9729-6)

NDC Information of Spironolactone

NDC Code 68788-9729-6
Proprietary Name Spironolactone
Package Description 60 TABLET in 1 BOTTLE (68788-9729-6)
Product NDC 68788-9729
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Spironolactone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121031
Marketing Category Name ANDA
Labeler Name Preferred 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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