NDC 53489-532

Atenolol and Chlorthalidone

Atenolol And Chlorthalidone

Atenolol and Chlorthalidone is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Mutual Pharmaceutical Company, Inc.. The primary component is Atenolol; Chlorthalidone.

Product ID53489-532_86da35ec-fbfa-4474-bf4b-a58d9c737a19
NDC53489-532
Product TypeHuman Prescription Drug
Proprietary NameAtenolol and Chlorthalidone
Generic NameAtenolol And Chlorthalidone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1993-04-29
Marketing CategoryANDA / ANDA
Application NumberANDA073582
Labeler NameMutual Pharmaceutical Company, Inc.
Substance NameATENOLOL; CHLORTHALIDONE
Active Ingredient Strength100 mg/1; mg/1
Pharm ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Thiazide-like Diuretic [EPC],Increased Diuresis [PE]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 53489-532-10

1000 TABLET in 1 BOTTLE, PLASTIC (53489-532-10)
Marketing Start Date1993-04-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53489-532-02 [53489053202]

Atenolol and Chlorthalidone TABLET
Marketing CategoryANDA
Application NumberANDA073582
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1993-04-29
Inactivation Date2019-11-27

NDC 53489-532-01 [53489053201]

Atenolol and Chlorthalidone TABLET
Marketing CategoryANDA
Application NumberANDA073582
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1993-04-29
Inactivation Date2019-11-27

NDC 53489-532-03 [53489053203]

Atenolol and Chlorthalidone TABLET
Marketing CategoryANDA
Application NumberANDA073582
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1993-04-29
Inactivation Date2019-11-27

NDC 53489-532-10 [53489053210]

Atenolol and Chlorthalidone TABLET
Marketing CategoryANDA
Application NumberANDA073582
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1993-04-29
Inactivation Date2019-11-27

NDC 53489-532-05 [53489053205]

Atenolol and Chlorthalidone TABLET
Marketing CategoryANDA
Application NumberANDA073582
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1993-04-29
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
ATENOLOL100 mg/1

OpenFDA Data

SPL SET ID:b4cfa459-c1c3-4fe2-ac2d-afeea2b96cca
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197382
  • 197383

    • Pharmacological Class

    • Adrenergic beta-Antagonists [MoA]
    • beta-Adrenergic Blocker [EPC]
    • Thiazide-like Diuretic [EPC]
    • Increased Diuresis [PE]

    NDC Crossover Matching brand name "Atenolol and Chlorthalidone" or generic name "Atenolol And Chlorthalidone"

    NDCBrand NameGeneric Name
    0378-2063Atenolol and Chlorthalidoneatenolol and chlorthalidone
    0378-2064Atenolol and Chlorthalidoneatenolol and chlorthalidone
    0591-5782Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    0591-5783Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    10135-733ATENOLOL AND CHLORTHALIDONEatenolol and chlorthalidone tablet
    10135-734ATENOLOL AND CHLORTHALIDONEatenolol and chlorthalidone tablet
    16714-936Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    16714-937Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    21695-743Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    21695-744Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    29300-400Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    29300-401Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    33261-942Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    43353-149Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    43353-985Atenolol and Chlorthalidoneatenolol and chlorthalidone
    53489-531Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    53489-532Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    55289-993Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    68071-3065Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    68788-9041Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    68788-9042Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    70518-2044Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    70518-2446Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    70518-3550Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    70710-1167Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    70710-1168Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    70771-1372Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    70771-1373Atenolol and ChlorthalidoneAtenolol and Chlorthalidone
    52427-382TENORETICAtenolol and Chlorthalidone
    52427-383TENORETICAtenolol and Chlorthalidone
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.