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Approved Drug Products containing 202231 listed in the FDA Orange Book. Original Data : FDA Website

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01 3FRESENIUS KABI USA

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01

Brand Name : LEVOTHYROXINE SODIUM

AAPS 2024
Not Confirmed
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Brand Name : LEVOTHYROXINE SODIUM

AAPS 2024
Not Confirmed
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Fresenius Kabi USA

Dosage Form : POWDER; INTRAVENOUS

Proprietary Name : LEVOTHYROXINE SODIUM

Dosage Strength : 100MCG/VIAL

Approval Date : 2011-06-24

Application Number : 202231

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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02

Brand Name : LEVOTHYROXINE SODIUM

AAPS 2024
Not Confirmed
arrow

Brand Name : LEVOTHYROXINE SODIUM

AAPS 2024
Not Confirmed
arrow

Fresenius Kabi USA

Dosage Form : POWDER; INTRAVENOUS

Proprietary Name : LEVOTHYROXINE SODIUM

Dosage Strength : 200MCG/VIAL

Approval Date : 2011-06-24

Application Number : 202231

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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03

Brand Name : LEVOTHYROXINE SODIUM

AAPS 2024
Not Confirmed
arrow

Brand Name : LEVOTHYROXINE SODIUM

AAPS 2024
Not Confirmed
arrow

Fresenius Kabi USA

Dosage Form : POWDER; INTRAVENOUS

Proprietary Name : LEVOTHYROXINE SODIUM

Dosage Strength : 500MCG/VIAL

Approval Date : 2011-06-24

Application Number : 202231

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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