NDC 31722-701

Losartan Potassium

Losartan Potassium

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

Product ID31722-701_9dab317a-e810-4e9d-b5cb-bb0181affc10
NDC31722-701
Product TypeHuman Prescription Drug
Proprietary NameLosartan Potassium
Generic NameLosartan Potassium
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2015-08-19
Marketing CategoryANDA / ANDA
Application NumberANDA203835
Labeler NameCamber Pharmaceuticals, Inc.
Substance NameLOSARTAN POTASSIUM
Active Ingredient Strength50 mg/1
Pharm ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 31722-701-05

500 TABLET, FILM COATED in 1 BOTTLE (31722-701-05)
Marketing Start Date2015-08-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 31722-701-05 [31722070105]

Losartan Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203835
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-19

NDC 31722-701-60 [31722070160]

Losartan Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203835
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-08-19

NDC 31722-701-10 [31722070110]

Losartan Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203835
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-08-19

NDC 31722-701-90 [31722070190]

Losartan Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203835
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-08-19

NDC 31722-701-30 [31722070130]

Losartan Potassium TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203835
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-08-19

Drug Details

Active Ingredients

IngredientStrength
LOSARTAN POTASSIUM50 mg/1

OpenFDA Data

SPL SET ID:cafd54e8-42a8-474c-8ea8-49ec74c2b0d3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 979485
  • 979492
  • 979480
  • Pharmacological Class

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

    Medicade Reported Pricing

    31722070190 LOSARTAN POTASSIUM 50 MG TAB

    Pricing Unit: EA | Drug Type:

    31722070130 LOSARTAN POTASSIUM 50 MG TAB

    Pricing Unit: EA | Drug Type:

    31722070110 LOSARTAN POTASSIUM 50 MG TAB

    Pricing Unit: EA | Drug Type:

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

    NDCBrand NameGeneric Name
    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
    68071-1516Losartan PotassiumLosartan Potassium
    68071-1518Losartan PotassiumLosartan Potassium
    68071-1517Losartan PotassiumLosartan Potassium
    68071-1684Losartan PotassiumLosartan Potassium
    68071-1986Losartan PotassiumLosartan Potassium
    68071-1912losartan potassiumlosartan potassium
    68071-1515Losartan PotassiumLosartan Potassium
    68071-1989Losartan PotassiumLosartan Potassium
    68071-3003Losartan PotassiumLosartan Potassium
    68071-2026Losartan PotassiumLosartan Potassium
    68071-3014Losartan PotassiumLosartan Potassium
    68071-4000Losartan PotassiumLosartan Potassium
    68071-4046Losartan PotassiumLosartan Potassium
    68071-3102Losartan PotassiumLosartan Potassium
    68071-4019Losartan PotassiumLosartan Potassium
    68071-3293Losartan PotassiumLosartan Potassium
    68071-3139Losartan PotassiumLosartan Potassium
    68071-4059Losartan PotassiumLosartan Potassium
    68071-3301Losartan PotassiumLosartan Potassium
    68071-4244Losartan potassiumLosartan potassium
    68071-3216Losartan PotassiumLosartan Potassium
    68071-4141Losartan PotassiumLosartan Potassium
    68071-4248Losartan potassiumLosartan potassium
    68071-4380Losartan PotassiumLosartan Potassium
    68071-4036Losartan potassiumLosartan potassium
    68071-4062Losartan potassiumLosartan potassium
    68071-4471Losartan PotassiumLosartan Potassium
    68071-4399Losartan PotassiumLosartan Potassium
    68071-4454Losartan PotassiumLosartan Potassium

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