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FDA ANDA · ANDA211082

RANOLAZINE

Sponsor: GLENMARK PHARMS LTD

APPLICATION
ANDA211082
TYPE
ANDA
ORIGINAL APPROVAL
2019-07-05
LATEST ACTION
2020-01-29
ROUTE
ORAL
DOSAGE FORM
TABLET, EXTENDED RELEASE
MARKETING STATUS
Prescription

Products

RANOLAZINEPrescription
RANOLAZINE 1GM · TABLET, EXTENDED RELEASE · ORAL
RANOLAZINEPrescription
RANOLAZINE 500MG · TABLET, EXTENDED RELEASE · ORAL

Approval history

2020-01-29Labeling · Supplement 2 · standardAP
2020-01-29Labeling · Supplement 1 · standardAP
2019-07-05UNKNOWN · Original · standardAP
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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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