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FDA ANDA · ANDA208749

LEVOTHYROXINE SODIUM

levothyroxine sodium anhydrous

Sponsor: MAIA PHARMS INC

APPLICATION
ANDA208749
TYPE
ANDA
ORIGINAL APPROVAL
2018-12-21
LATEST ACTION
2018-12-21
ROUTE
INTRAVENOUS
DOSAGE FORM
POWDER
MARKETING STATUS
Prescription

Products

LEVOTHYROXINE SODIUMPrescription
LEVOTHYROXINE SODIUM 200MCG/VIAL · POWDER · INTRAVENOUS
LEVOTHYROXINE SODIUMPrescription
LEVOTHYROXINE SODIUM 500MCG/VIAL · POWDER · INTRAVENOUS
LEVOTHYROXINE SODIUMPrescription
LEVOTHYROXINE SODIUM 100MCG/VIAL · POWDER · INTRAVENOUS

Approval history

2018-12-21UNKNOWN · Original · standardAP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

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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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