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Approved Drug Products containing 22321 listed in the FDA Orange Book. Original Data : FDA Website

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01 6ALPHARMA PHARMS

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PharmaCompass

01

Brand Name : EMBEDA

Luxepack
Not Confirmed
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Brand Name : EMBEDA

Luxepack
Not Confirmed
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Actavis Inc

Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

Proprietary Name : EMBEDA

Dosage Strength : 50MG;2MG **Federal Regis...

Approval Date : 2009-08-13

Application Number : 22321

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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02

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Actavis Inc

Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

Proprietary Name : EMBEDA

Dosage Strength : 20MG;0.8MG **Federal Reg...

Approval Date : 2009-08-13

Application Number : 22321

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Actavis Inc

Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

Proprietary Name : EMBEDA

Dosage Strength : 100MG;4MG **Federal Regi...

Approval Date : 2009-08-13

Application Number : 22321

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Actavis Inc

Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

Proprietary Name : EMBEDA

Dosage Strength : 60MG;2.4MG **Federal Reg...

Approval Date : 2009-08-13

Application Number : 22321

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Actavis Inc

Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

Proprietary Name : EMBEDA

Dosage Strength : 30MG;1.2MG **Federal Reg...

Approval Date : 2009-08-13

Application Number : 22321

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

06

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Brand Name : EMBEDA

Luxepack
Not Confirmed
arrow

Actavis Inc

Dosage Form : CAPSULE, EXTENDED RELEASE; ORA...

Proprietary Name : EMBEDA

Dosage Strength : 80MG;3.2MG **Federal Reg...

Approval Date : 2009-08-13

Application Number : 22321

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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