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Approved Drug Products containing 91624 listed in the FDA Orange Book. Original Data : FDA Website

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01 4LANNETT CO INC

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01

Brand Name : ATORVASTATIN CALCIUM

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Brand Name : ATORVASTATIN CALCIUM

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Lannett Company, Inc.

Dosage Form : TABLET; ORAL

Proprietary Name : ATORVASTATIN CALCIUM

Dosage Strength : EQ 80MG BASE

Approval Date : 2013-04-05

Application Number : 91624

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : ATORVASTATIN CALCIUM

Luxepack
Not Confirmed
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Brand Name : ATORVASTATIN CALCIUM

Luxepack
Not Confirmed
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Lannett Company, Inc.

Dosage Form : TABLET; ORAL

Proprietary Name : ATORVASTATIN CALCIUM

Dosage Strength : EQ 20MG BASE

Approval Date : 2013-04-05

Application Number : 91624

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : ATORVASTATIN CALCIUM

Luxepack
Not Confirmed
arrow

Brand Name : ATORVASTATIN CALCIUM

Luxepack
Not Confirmed
arrow

Lannett Company, Inc.

Dosage Form : TABLET; ORAL

Proprietary Name : ATORVASTATIN CALCIUM

Dosage Strength : EQ 40MG BASE

Approval Date : 2013-04-05

Application Number : 91624

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

Brand Name : ATORVASTATIN CALCIUM

Luxepack
Not Confirmed
arrow

Brand Name : ATORVASTATIN CALCIUM

Luxepack
Not Confirmed
arrow

Lannett Company, Inc.

Dosage Form : TABLET; ORAL

Proprietary Name : ATORVASTATIN CALCIUM

Dosage Strength : EQ 10MG BASE

Approval Date : 2013-04-05

Application Number : 91624

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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