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    Ferndale Laboratories, Inc.

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    01 1CHLORZOXAZONE

    02 1DEXTROAMPHETAMINE SULFATE

    03 3DIAZEPAM

    04 1HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    05 1MEPROBAMATE

    06 1METHOCARBAMOL

    07 2PHENDIMETRAZINE TARTRATE

    08 1PHENTERMINE HYDROCHLORIDE

    09 1PREDNISOLONE

    10 1PREDNISONE

    11 2RAUWOLFIA SERPENTINA ROOT

    12 1THEOPHYLLINE

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    01

    Brand Name : STRIFON FORTE DSC

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    Brand Name : STRIFON FORTE DSC

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    RLD : No

    TE Code :

    CHLORZOXAZONE

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : STRIFON FORTE DSC

    Dosage Strength : 500MG

    Approval Date : 1988-12-23

    Application Number : 81008

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Brand Name : FERNDEX

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    RLD : No

    TE Code :

    DEXTROAMPHETAMINE SULFATE

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : FERNDEX

    Dosage Strength : 5MG

    Approval Date : 1982-01-01

    Application Number : 84001

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : DIAZEPAM

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    RLD : No

    TE Code :

    DIAZEPAM

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : DIAZEPAM

    Dosage Strength : 2MG

    Approval Date : 1987-04-01

    Application Number : 70903

    RX/OTC/DISCN : DISCN

    RLD : No

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    Brand Name : DIAZEPAM

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    RLD : No

    TE Code :

    DIAZEPAM

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : DIAZEPAM

    Dosage Strength : 5MG

    Approval Date : 1987-04-01

    Application Number : 70904

    RX/OTC/DISCN : DISCN

    RLD : No

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    Brand Name : DIAZEPAM

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    RLD : No

    TE Code :

    DIAZEPAM

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : DIAZEPAM

    Dosage Strength : 10MG

    Approval Date : 1987-04-01

    Application Number : 70905

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    Brand Name : PRAMOSONE

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    RLD : No

    TE Code :

    HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE

    Ferndale Laboratories, Inc.

    Dosage Form : LOTION; TOPICAL

    Proprietary Name : PRAMOSONE

    Dosage Strength : 0.5%;1%

    Approval Date : 1982-01-01

    Application Number : 83213

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : AMOSENE

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    RLD : No

    TE Code :

    MEPROBAMATE

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMOSENE

    Dosage Strength : 400MG

    Approval Date : 1982-01-01

    Application Number : 84030

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    Brand Name : DELAXIN

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    RLD : No

    TE Code :

    METHOCARBAMOL

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : DELAXIN

    Dosage Strength : 500MG

    Approval Date : 1982-01-01

    Application Number : 85454

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    Brand Name : ADPHEN

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    RLD : No

    TE Code :

    PHENDIMETRAZINE TARTRATE

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : ADPHEN

    Dosage Strength : 35MG

    Approval Date : 1982-01-01

    Application Number : 83655

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Brand Name : PHENDIMETRAZINE TART...

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    RLD : No

    TE Code :

    PHENDIMETRAZINE TARTRATE

    Ferndale Laboratories, Inc.

    Dosage Form : TABLET; ORAL

    Proprietary Name : PHENDIMETRAZINE TARTRATE

    Dosage Strength : 35MG

    Approval Date : 1983-09-15

    Application Number : 86834

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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