NDC 62980-502

LOSARTAN POTASSIUM 50 mg

Losartan Potassium

LOSARTAN POTASSIUM 50 mg is a Oral; Oral; Oral; Oral; Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Vivimed Labs Limited. The primary component is Losartan Potassium.

Product ID62980-502_c86f6112-1ed8-44a7-a240-3b5fed85cc67
NDC62980-502
Product TypeHuman Prescription Drug
Proprietary NameLOSARTAN POTASSIUM 50 mg
Generic NameLosartan Potassium
Dosage FormTablet, Film Coated
Route of AdministrationORAL; ORAL; ORAL; ORAL; ORAL
Marketing Start Date2014-03-11
Marketing CategoryANDA / ANDA
Application NumberANDA090382
Labeler NameVivimed Labs Limited
Substance NameLOSARTAN POTASSIUM
Active Ingredient Strength50 mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 62980-502-01

30 TABLET, FILM COATED in 1 BOTTLE (62980-502-01)
Marketing Start Date2014-03-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62980-502-01 [62980050201]

LOSARTAN POTASSIUM 50 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090382
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11
Marketing End Date2019-11-26

NDC 62980-502-05 [62980050205]

LOSARTAN POTASSIUM 50 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090382
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11
Marketing End Date2019-11-26

NDC 62980-502-02 [62980050202]

LOSARTAN POTASSIUM 50 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090382
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11
Marketing End Date2019-11-26

NDC 62980-502-03 [62980050203]

LOSARTAN POTASSIUM 50 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090382
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-03-11
Marketing End Date2019-11-26

Drug Details

Active Ingredients

IngredientStrength
LOSARTAN POTASSIUM50 mg/1

OpenFDA Data

SPL SET ID:9937ccb7-32bd-4fd4-81a0-bedad6810efe
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 979485
  • 979492
  • 979480
  • Pharmacological Class

    • Angiotensin 2 Receptor Antagonists [MoA]
    • Angiotensin 2 Receptor Blocker [EPC]

    NDC Crossover Matching brand name "LOSARTAN POTASSIUM 50 mg" or generic name "Losartan Potassium"

    NDCBrand NameGeneric Name
    23155-645LOSARTAN POTASSIUM 50 mgLOSARTAN POTASSIUM 50 mg
    62980-502LOSARTAN POTASSIUM 50 mgLOSARTAN POTASSIUM 50 mg
    64380-934LOSARTAN POTASSIUM 50 mgLOSARTAN POTASSIUM 50 mg
    68071-5146LOSARTAN POTASSIUM 50 mgLOSARTAN POTASSIUM 50 mg
    70518-2530LOSARTAN POTASSIUM 50 mgLOSARTAN POTASSIUM 50 mg
    72789-164LOSARTAN POTASSIUM 50 mgLOSARTAN POTASSIUM 50 mg
    70934-781LOSARTAN POTASSIUM 50 mgLOSARTAN POTASSIUM 50 mg
    0006-0951COZAARlosartan potassium
    0006-0952COZAARlosartan potassium
    0006-0960COZAARlosartan potassium
    0054-0123Losartan PotassiumLosartan Potassium
    0054-0124Losartan PotassiumLosartan Potassium
    0054-0125Losartan PotassiumLosartan Potassium
    0093-7364Losartan PotassiumLosartan Potassium
    0093-7365Losartan PotassiumLosartan Potassium
    0093-7366Losartan PotassiumLosartan Potassium
    0179-0200Losartan PotassiumLosartan Potassium
    0179-0202Losartan PotassiumLosartan Potassium
    0179-0203Losartan PotassiumLosartan Potassium
    0615-7604Losartan PotassiumLosartan Potassium
    0615-7605Losartan PotassiumLosartan Potassium
    0615-7606Losartan PotassiumLosartan Potassium
    0615-7958Losartan PotassiumLosartan Potassium
    0615-7959Losartan PotassiumLosartan Potassium
    0615-7960Losartan PotassiumLosartan Potassium
    0615-8207Losartan PotassiumLosartan Potassium
    0615-8208Losartan PotassiumLosartan Potassium
    0615-8209Losartan PotassiumLosartan Potassium
    0781-5700Losartan potassiumlosartan potassium
    0781-5701Losartan potassiumlosartan potassium
    0781-5702Losartan potassiumlosartan potassium

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