NDC 53808-0796

Spironolactone

Spironolactone

Spironolactone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by State Of Florida Doh Central Pharmacy. The primary component is Spironolactone.

Product ID53808-0796_e1a6cafb-dc98-4630-9cbe-519e08ab1691
NDC53808-0796
Product TypeHuman Prescription Drug
Proprietary NameSpironolactone
Generic NameSpironolactone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-07-01
Marketing CategoryANDA / ANDA
Application NumberANDA040353
Labeler NameState of Florida DOH Central Pharmacy
Substance NameSPIRONOLACTONE
Active Ingredient Strength25 mg/1
Pharm ClassesAldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 53808-0796-1

30 TABLET in 1 BLISTER PACK (53808-0796-1)
Marketing Start Date2009-07-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53808-0796-1 [53808079601]

Spironolactone TABLET
Marketing CategoryANDA
Application NumberANDA040353
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-07-01
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SPIRONOLACTONE25 mg/1

Pharmacological Class

  • Aldosterone Antagonist [EPC]
  • Aldosterone Antagonists [MoA]

NDC Crossover Matching brand name "Spironolactone" or generic name "Spironolactone"

NDCBrand NameGeneric Name
0228-2672SpironolactoneSpironolactone
0228-2673SpironolactoneSpironolactone
0228-2803SpironolactoneSpironolactone
0378-0243Spironolactonespironolactone
0378-0437Spironolactonespironolactone
0378-2146Spironolactonespironolactone
0603-5763Spironolactonespironolactone
0603-5764Spironolactonespironolactone
0603-5765Spironolactonespironolactone
0615-1535Spironolactonespironolactone
0615-5592Spironolactonespironolactone
0615-6591Spironolactonespironolactone
0615-8031Spironolactonespironolactone
0615-8178Spironolactonespironolactone
0615-8221Spironolactonespironolactone
0781-1599SpironolactoneSpironolactone
68071-1992SpironolactoneSpironolactone
68071-3112SpironolactoneSpironolactone
68071-3375SpironolactoneSpironolactone
68071-4073SpironolactoneSpironolactone
68071-4374SpironolactoneSpironolactone
68084-207SpironolactoneSpironolactone
68084-208SpironolactoneSpironolactone
68084-206SpironolactoneSpironolactone
68151-2776SpironolactoneSpironolactone
68382-661spironolactonespironolactone
68382-662spironolactonespironolactone
68382-660spironolactonespironolactone
68788-7051SpironolactoneSpironolactone
68788-6332SpironolactoneSpironolactone
68788-6895SpironolactoneSpironolactone
68788-6900SpironolactoneSpironolactone
68788-9227SpironolactoneSpironolactone
68788-7019SpironolactoneSpironolactone
68788-7258SpironolactoneSpironolactone
68788-7297SpironolactoneSpironolactone
68788-9124SpironolactoneSpironolactone
68788-9729SpironolactoneSpironolactone
70518-0455SpironolactoneSpironolactone
70518-0563SpironolactoneSpironolactone
70518-0603SpironolactoneSpironolactone
70518-0630SpironolactoneSpironolactone
70518-1334SpironolactoneSpironolactone
70518-0665SpironolactoneSpironolactone
70518-1314SpironolactoneSpironolactone
70518-1746SpironolactoneSpironolactone
70518-1742SpironolactoneSpironolactone
70771-1029spironolactonespironolactone
70771-1028spironolactonespironolactone
70771-1027spironolactonespironolactone

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.