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Spironolactone - 51079-103-19 - (spironolactone)

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Drug Information of Spironolactone

Product NDC: 51079-103
Proprietary Name: Spironolactone
Non Proprietary Name: spironolactone
Active Ingredient(s): 25    mg/1 & nbsp;   spironolactone
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Spironolactone

Product NDC: 51079-103
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040424
Marketing Category: ANDA
Start Marketing Date: 20110204

Package Information of Spironolactone

Package NDC: 51079-103-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-103-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-103-17)

NDC Information of Spironolactone

NDC Code 51079-103-19
Proprietary Name Spironolactone
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-103-19) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-103-17)
Product NDC 51079-103
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name spironolactone
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110204
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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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