NDC 70518-0862

Losatan Potassium

Losatan Potassium

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

Product ID70518-0862_5e9924be-4d79-324a-e053-2a91aa0a8ec1
NDC70518-0862
Product TypeHuman Prescription Drug
Proprietary NameLosatan Potassium
Generic NameLosatan Potassium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-11-22
Marketing CategoryANDA / ANDA
Application NumberANDA090428
Labeler NameREMEDYREPACK INC.
Substance NameLOSARTAN POTASSIUM
Active Ingredient Strength100 mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 70518-0862-0

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0862-0)
Marketing Start Date2017-11-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-0862-0 [70518086200]

Losatan Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090428
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-11-22
Marketing End Date2020-05-06

Drug Details

Active Ingredients

IngredientStrength
LOSARTAN POTASSIUM100 mg/1

OpenFDA Data

SPL SET ID:6f47b544-a451-4689-ab51-895b039c55cb
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 979480
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Losatan Potassium" or generic name "Losatan Potassium"

    NDCBrand NameGeneric Name
    46708-445Losatan PotassiumLosatan Potassium
    46708-446Losatan PotassiumLosatan Potassium
    46708-447Losatan PotassiumLosatan Potassium
    51655-258Losatan PotassiumLosatan Potassium
    62332-027Losatan PotassiumLosatan Potassium
    62332-028Losatan PotassiumLosatan Potassium
    62332-029Losatan PotassiumLosatan Potassium
    70518-0862Losatan PotassiumLosatan Potassium

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