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FDA ANDA · ANDA207807
AMLODIPINE AND OLMESARTAN MEDOXOMIL
Sponsor: GLENMARK PHARMS LTD
APPLICATION
ANDA207807
TYPE
ANDA
ORIGINAL APPROVAL
2017-07-05
LATEST ACTION
2021-01-04
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
AMLODIPINE AND OLMESARTAN MEDOXOMILDiscontinued
AMLODIPINE BESYLATE EQ 10MG BASE, OLMESARTAN MEDOXOMIL 20MG · TABLET · ORAL
AMLODIPINE AND OLMESARTAN MEDOXOMILDiscontinued
AMLODIPINE BESYLATE EQ 5MG BASE, OLMESARTAN MEDOXOMIL 20MG · TABLET · ORAL
AMLODIPINE AND OLMESARTAN MEDOXOMILDiscontinued
AMLODIPINE BESYLATE EQ 10MG BASE, OLMESARTAN MEDOXOMIL 40MG · TABLET · ORAL
AMLODIPINE AND OLMESARTAN MEDOXOMILDiscontinued
AMLODIPINE BESYLATE EQ 5MG BASE, OLMESARTAN MEDOXOMIL 40MG · TABLET · ORAL
Approval history
2021-01-04Labeling · Supplement 3 · standardAP
2017-07-05UNKNOWN · Original · standardAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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