← FDA DRUG APPROVALS

FDA ANDA · ANDA201380

AMLODIPINE BESYLATE

Sponsor: GRAVITI PHARMS

APPLICATION
ANDA201380
TYPE
ANDA
ORIGINAL APPROVAL
2012-04-13
LATEST ACTION
2026-02-17
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription

Products

AMLODIPINE BESYLATEPrescription
AMLODIPINE BESYLATE EQ 10MG BASE · TABLET · ORAL
AMLODIPINE BESYLATEPrescription
AMLODIPINE BESYLATE EQ 2.5MG BASE · TABLET · ORAL
AMLODIPINE BESYLATEPrescription
AMLODIPINE BESYLATE EQ 5MG BASE · TABLET · ORAL

Approval history

2026-02-17Manufacturing (CMC) · Supplement 23 · unknownAP
2026-01-26Manufacturing (CMC) · Supplement 22 · unknownAP
2023-06-07Labeling · Supplement 17 · standardAP
2018-04-03Labeling · Supplement 7 · standardAP
2015-12-03Labeling · Supplement 5 · standardAP
2014-09-19Labeling · Supplement 2 · standardAP
2012-04-13UNKNOWN · OriginalAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

Pharma industryGMP disciplineFDA drug shortagesFDA enforcement & recalls

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.

Weekly Briefing

Get the Weekly GxP Briefing

Curated regulatory intelligence — enforcement, recalls, guidance, and quality signals — in one practitioner-grade email each week. Free.

Read a past issue →