NDC 59762-1540

amlodipine besylate

Amlodipine Besylate

amlodipine besylate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Greenstone Llc. The primary component is Amlodipine Besylate.

Product ID59762-1540_4b488534-377e-4fbb-93fb-3bd140782d3a
NDC59762-1540
Product TypeHuman Prescription Drug
Proprietary Nameamlodipine besylate
Generic NameAmlodipine Besylate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-03-23
Marketing End Date2020-04-30
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA019787
Labeler NameGreenstone LLC
Substance NameAMLODIPINE BESYLATE
Active Ingredient Strength10 mg/1
Pharm ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
NDC Exclude FlagN

Packaging

NDC 59762-1540-1

90 TABLET in 1 BOTTLE (59762-1540-1)
Marketing Start Date2007-03-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59762-1540-4 [59762154004]

amlodipine besylate TABLET
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA019787
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-23
Marketing End Date2018-06-30

NDC 59762-1540-3 [59762154003]

amlodipine besylate TABLET
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA019787
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-23
Marketing End Date2020-04-30

NDC 59762-1540-6 [59762154006]

amlodipine besylate TABLET
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA019787
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-09-30
Marketing End Date2012-06-05

NDC 59762-1540-1 [59762154001]

amlodipine besylate TABLET
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA019787
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-23
Marketing End Date2020-03-31

NDC 59762-1540-2 [59762154002]

amlodipine besylate TABLET
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA019787
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2007-03-23
Marketing End Date2020-04-30

NDC 59762-1540-5 [59762154005]

amlodipine besylate TABLET
Marketing CategoryNDA AUTHORIZED GENERIC
Application NumberNDA019787
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2012-06-05
Marketing End Date2019-07-15

Drug Details

Active Ingredients

IngredientStrength
AMLODIPINE BESYLATE10 mg/1

OpenFDA Data

SPL SET ID:180ee374-24f2-4b9c-9d54-8815f2b1dc9b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 308136
  • 308135
  • 197361
  • UPC Code
  • 0359762152022
  • 0359762153036
  • 0359762154033
  • Pharmacological Class

    • Calcium Channel Antagonists [MoA]
    • Dihydropyridine Calcium Channel Blocker [EPC]
    • Dihydropyridines [CS]

    Medicade Reported Pricing

    59762154005 AMLODIPINE BESYLATE 10 MG TAB

    Pricing Unit: EA | Drug Type:

    59762154004 AMLODIPINE BESYLATE 10 MG TAB

    Pricing Unit: EA | Drug Type:

    59762154003 AMLODIPINE BESYLATE 10 MG TAB

    Pricing Unit: EA | Drug Type:

    59762154002 AMLODIPINE BESYLATE 10 MG TAB

    Pricing Unit: EA | Drug Type:

    59762154001 AMLODIPINE BESYLATE 10 MG TAB

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "amlodipine besylate" or generic name "Amlodipine Besylate"

    NDCBrand NameGeneric Name
    0054-0100Amlodipine BesylateAmlodipine Besylate
    0054-0101Amlodipine BesylateAmlodipine Besylate
    0054-0102Amlodipine BesylateAmlodipine Besylate
    0093-0083Amlodipine BesylateAmlodipine Besylate
    0093-7167Amlodipine BesylateAmlodipine Besylate
    0093-7168Amlodipine BesylateAmlodipine Besylate
    0143-9959Amlodipine besylateAmlodipine besylate
    0143-9960Amlodipine besylateAmlodipine besylate
    0143-9961Amlodipine besylateAmlodipine besylate
    0179-0210Amlodipine BesylateAmlodipine Besylate
    0179-0211Amlodipine BesylateAmlodipine Besylate
    0179-0213Amlodipine BesylateAmlodipine Besylate
    0378-5208Amlodipine Besylateamlodipine besylate
    0378-5209Amlodipine Besylateamlodipine besylate
    0378-5210Amlodipine Besylateamlodipine besylate
    0480-0083Amlodipine BesylateAmlodipine Besylate
    0480-7167Amlodipine BesylateAmlodipine Besylate
    0480-7168Amlodipine BesylateAmlodipine Besylate
    0603-2108Amlodipine Besylateamlodipine besylate
    0603-2109Amlodipine Besylateamlodipine besylate
    0603-2110Amlodipine Besylateamlodipine besylate
    0615-6577Amlodipine Besylateamlodipine besylate
    0615-6578Amlodipine Besylateamlodipine besylate
    0615-6582Amlodipine BesylateAmlodipine
    0615-7939Amlodipine BesylateAmlodipine Besylate
    0615-7941AMLODIPINE BESYLATEAMLODIPINE BESYLATE
    0615-7942Amlodipine BesylateAmlodipine Besylate
    0615-8199Amlodipine BesylateAmlodipine Besylate
    0615-8200Amlodipine BesylateAmlodipine Besylate
    0615-8201Amlodipine BesylateAmlodipine Besylate
    0615-8282AMLODIPINE BESYLATEAMLODIPINE BESYLATE
    67544-979Amlodipine BesylateAmlodipine Besylate
    67544-993Amlodipine BesylateAmlodipine Besylate
    67877-198Amlodipine BesylateAmlodipine Besylate
    67877-197Amlodipine BesylateAmlodipine Besylate
    67877-199Amlodipine BesylateAmlodipine Besylate
    68071-1902Amlodipine BesylateAmlodipine Besylate
    68071-1974AMLODIPINE BESYLATEAMLODIPINE BESYLATE
    68071-1924Amlodipine BesylateAmlodipine Besylate
    68071-1903Amlodipine BesylateAmlodipine Besylate
    68071-3188AMLODIPINE BESYLATEAMLODIPINE BESYLATE
    68071-1980AMLODIPINE BESYLATEAMLODIPINE BESYLATE
    68071-4251Amlodipine BesylateAmlodipine Besylate
    68071-3327AMLODIPINE BESYLATEAMLODIPINE BESYLATE
    68071-4776Amlodipine BesylateAmlodipine Besylate
    68151-0995Amlodipine BesylateAmlodipine Besylate
    68180-720Amlodipine BesylateAmlodipine Besylate
    68180-750Amlodipine BesylateAmlodipine Besylate
    68180-721Amlodipine BesylateAmlodipine Besylate
    68180-752Amlodipine BesylateAmlodipine Besylate

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