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FDA ANDA · ANDA216427

FAMOTIDINE

Sponsor: AMNEAL

APPLICATION
ANDA216427
TYPE
ANDA
ORIGINAL APPROVAL
2022-08-04
LATEST ACTION
2022-08-04
ROUTE
ORAL
DOSAGE FORM
FOR SUSPENSION
MARKETING STATUS
Prescription

Products

FAMOTIDINEPrescription
FAMOTIDINE 40MG/5ML · FOR SUSPENSION · ORAL

Approval history

2022-08-04UNKNOWN · 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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