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FDA ANDA · ANDA210339

PROPAFENONE HYDROCHLORIDE

propafenone

Sponsor: SINOTHERAPEUTICS INC

APPLICATION
ANDA210339
TYPE
ANDA
ORIGINAL APPROVAL
2019-01-04
LATEST ACTION
2019-01-04
ROUTE
ORAL
DOSAGE FORM
CAPSULE, EXTENDED RELEASE
MARKETING STATUS
Prescription

Products

PROPAFENONE HYDROCHLORIDEPrescription
PROPAFENONE HYDROCHLORIDE 325MG · CAPSULE, EXTENDED RELEASE · ORAL
PROPAFENONE HYDROCHLORIDEPrescription
PROPAFENONE HYDROCHLORIDE 425MG · CAPSULE, EXTENDED RELEASE · ORAL
PROPAFENONE HYDROCHLORIDEPrescription
PROPAFENONE HYDROCHLORIDE 225MG · CAPSULE, EXTENDED RELEASE · ORAL

Approval history

2019-01-04UNKNOWN · 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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