NDC 62332-050

Losartan Potassium and Hydrochlorothiazide

Losartan Potassium And Hydrochlorothiazide

Losartan Potassium and Hydrochlorothiazide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Alembic Pharmaceuticals Inc.. The primary component is Losartan Potassium; Hydrochlorothiazide.

Product ID62332-050_288ce6a0-4332-4b93-b879-77781132bcc3
NDC62332-050
Product TypeHuman Prescription Drug
Proprietary NameLosartan Potassium and Hydrochlorothiazide
Generic NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2016-05-23
Marketing CategoryANDA / ANDA
Application NumberANDA091617
Labeler NameAlembic Pharmaceuticals Inc.
Substance NameLOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
Active Ingredient Strength100 mg/1; mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 62332-050-10

100 BLISTER PACK in 1 CARTON (62332-050-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2016-05-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62332-050-91 [62332005091]

Losartan Potassium and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091617
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-05-23

NDC 62332-050-10 [62332005010]

Losartan Potassium and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091617
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-05-23

NDC 62332-050-90 [62332005090]

Losartan Potassium and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091617
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-05-23

NDC 62332-050-30 [62332005030]

Losartan Potassium and Hydrochlorothiazide TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091617
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-05-23

Drug Details

Active Ingredients

IngredientStrength
LOSARTAN POTASSIUM100 mg/1

OpenFDA Data

SPL SET ID:acecced9-2a61-435d-b7d4-b151cb7b7e5d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 979468
  • 979471
  • 979464
  • UPC Code
  • 0362332049301
  • 0362332050307
  • 0362332048304
  • Pharmacological Class

    • Angiotensin 2 Receptor Antagonists [MoA]
    • Angiotensin 2 Receptor Blocker [EPC]
    • Increased Diuresis [PE]
    • Thiazide Diuretic [EPC]
    • Thiazides [CS]

    Medicade Reported Pricing

    62332005091 LOSARTAN-HYDROCHLOROTHIAZIDE 100-25 MG TAB

    Pricing Unit: EA | Drug Type:

    62332005090 LOSARTAN-HYDROCHLOROTHIAZIDE 100-25 MG TAB

    Pricing Unit: EA | Drug Type:

    62332005030 LOSARTAN-HYDROCHLOROTHIAZIDE 100-25 MG TAB

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Losartan Potassium and Hydrochlorothiazide" or generic name "Losartan Potassium And Hydrochlorothiazide"

    NDCBrand NameGeneric Name
    0054-0126Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    0054-0127Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    0054-0277Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    0093-7367Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    0093-7368Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    0093-7369Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    0781-5204Losartan potassium and hydrochlorothiazideLosartan potassium and hydrochlorothiazide tablets
    0781-5206Losartan potassium and hydrochlorothiazideLosartan potassium and hydrochlorothiazide tablets
    0781-5207Losartan potassium and hydrochlorothiazideLosartan potassium and hydrochlorothiazide tablets
    68071-1916Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-1947Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-1613Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-2177Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-1690Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-1952Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4222Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4159Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4640Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4518Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4493Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4699Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4187Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4448Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68071-4768Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68180-216Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68180-215Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68180-217Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68258-6031Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68258-6040LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
    68382-143LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
    68382-142LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
    68645-412Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68788-6329Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68788-6452Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68788-6812Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    68788-9461Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    70518-0112Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    70518-0354Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    70518-0602Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    70518-0786Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    70518-1682Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    70518-1526Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    70518-1943Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    71335-0152Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    71335-0558Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    71335-0411Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    71335-1062Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    71335-1025Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    71335-0916Losartan Potassium and HydrochlorothiazideLosartan Potassium and Hydrochlorothiazide
    0781-5817losartan potassium and hydrochlorothiazidelosartan potassium and hydrochlorothiazide

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