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FDA ANDA · ANDA217782

OXCARBAZEPINE

Sponsor: KANCHAN HLTHCARE

APPLICATION
ANDA217782
TYPE
ANDA
ORIGINAL APPROVAL
2024-02-14
LATEST ACTION
2026-07-13
ROUTE
ORAL
DOSAGE FORM
SUSPENSION
MARKETING STATUS
Prescription

Products

OXCARBAZEPINEPrescription
OXCARBAZEPINE 300MG/5ML · SUSPENSION · ORAL

Approval history

2026-07-13Labeling · Supplement 2 · standardAP
2024-02-14UNKNOWN · Original · standardAP
VIEW ON DRUGS@FDA ↗

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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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