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FDA ANDA · ANDA210924

METHYLPHENIDATE

Sponsor: ACTAVIS ELIZABETH

APPLICATION
ANDA210924
TYPE
ANDA
ORIGINAL APPROVAL
2020-06-19
LATEST ACTION
2020-06-19
ROUTE
ORAL
DOSAGE FORM
TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE
MARKETING STATUS
Prescription

Products

METHYLPHENIDATEPrescription
METHYLPHENIDATE 17.3MG · TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE · ORAL
METHYLPHENIDATEPrescription
METHYLPHENIDATE 25.9MG · TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE · ORAL
METHYLPHENIDATEPrescription
METHYLPHENIDATE 8.6MG · TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE · ORAL

Approval history

2020-06-19UNKNOWN · Original · standardLetterAP
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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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