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    Aurolife Pharma LLC

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    01 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    02 3ACETAMINOPHEN; CODEINE PHOSPHATE

    03 6ACETAMINOPHEN; HYDROCODONE BITARTRATE

    04 4ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

    05 13AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE

    06 2AMPHETAMINE SULFATE

    07 2CHLORPHENIRAMINE MALEATE

    08 5CLORAZEPATE DIPOTASSIUM

    09 8DEXMETHYLPHENIDATE HYDROCHLORIDE

    10 2DEXTROAMPHETAMINE SULFATE

    11 2DICLOFENAC SODIUM

    12 2HYDROCHLOROTHIAZIDE

    13 1HYDROCODONE BITARTRATE; IBUPROFEN

    14 3HYDROMORPHONE HYDROCHLORIDE

    15 2METHADONE HYDROCHLORIDE

    16 7METHYLPHENIDATE HYDROCHLORIDE

    17 2OMEPRAZOLE; SODIUM BICARBONATE

    18 5OXYCODONE HYDROCHLORIDE

    19 2OXYMORPHONE HYDROCHLORIDE

    20 2PHENTERMINE HYDROCHLORIDE

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    01

    Brand Name : BUTALBITAL, ACETAMIN...

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    ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    Aurolife Pharma LLC

    Dosage Form : CAPSULE;ORAL

    Brand Name : BUTALBITAL, ACETAMINOPHEN...

    Dosage Strength : 325MG;50MG;40MG

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    Approval Date : 2018-09-26

    Application Number : 204733

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : ACETAMINOPHEN AND CO...

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    ACETAMINOPHEN; CODEINE PHOSPHATE

    Aurolife Pharma LLC

    Dosage Form : TABLET;ORAL

    Brand Name : ACETAMINOPHEN AND CODEINE...

    Dosage Strength : 300MG;15MG

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    Approval Date : 2013-04-15

    Application Number : 202800

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : ACETAMINOPHEN AND CO...

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    Dosage Form : TABLET;ORAL

    Brand Name : ACETAMINOPHEN AND CODEINE...

    Dosage Strength : 300MG;30MG

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    Approval Date : 2013-04-15

    Application Number : 202800

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    Registration Country : USA

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    04

    Brand Name : ACETAMINOPHEN AND CO...

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    Aurolife Pharma LLC

    Dosage Form : TABLET;ORAL

    Brand Name : ACETAMINOPHEN AND CODEINE...

    Dosage Strength : 300MG;60MG

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    Approval Date : 2013-04-15

    Application Number : 202800

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : HYDROCODONE BITARTRA...

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    Regulatory Info : RX

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    ACETAMINOPHEN; HYDROCODONE BITARTRATE

    Aurolife Pharma LLC

    Dosage Form : TABLET;ORAL

    Brand Name : HYDROCODONE BITARTRATE AN...

    Dosage Strength : 325MG;5MG

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    Approval Date : 2012-04-11

    Application Number : 201013

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : HYDROCODONE BITARTRA...

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    Regulatory Info : RX

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    ACETAMINOPHEN; HYDROCODONE BITARTRATE

    Aurolife Pharma LLC

    Dosage Form : TABLET;ORAL

    Brand Name : HYDROCODONE BITARTRATE AN...

    Dosage Strength : 325MG;7.5MG

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    Approval Date : 2012-04-11

    Application Number : 201013

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : HYDROCODONE BITARTRA...

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    Regulatory Info : RX

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    ACETAMINOPHEN; HYDROCODONE BITARTRATE

    Aurolife Pharma LLC

    Dosage Form : TABLET;ORAL

    Brand Name : HYDROCODONE BITARTRATE AN...

    Dosage Strength : 325MG;10MG

    Packaging :

    Approval Date : 2012-04-11

    Application Number : 201013

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : HYDROCODONE BITARTRA...

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    ACETAMINOPHEN; HYDROCODONE BITARTRATE

    Aurolife Pharma LLC

    Dosage Form : TABLET;ORAL

    Brand Name : HYDROCODONE BITARTRATE AN...

    Dosage Strength : 300MG;5MG

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    Approval Date : 2018-09-13

    Application Number : 207709

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : HYDROCODONE BITARTRA...

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    ACETAMINOPHEN; HYDROCODONE BITARTRATE

    Aurolife Pharma LLC

    Dosage Form : TABLET;ORAL

    Brand Name : HYDROCODONE BITARTRATE AN...

    Dosage Strength : 300MG;7.5MG

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    Approval Date : 2018-09-13

    Application Number : 207709

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    Registration Country : USA

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    Brand Name : HYDROCODONE BITARTRA...

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    ACETAMINOPHEN; HYDROCODONE BITARTRATE

    Aurolife Pharma LLC

    Dosage Form : TABLET;ORAL

    Brand Name : HYDROCODONE BITARTRATE AN...

    Dosage Strength : 300MG;10MG

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    Approval Date : 2018-09-13

    Application Number : 207709

    Regulatory Info : RX

    Registration Country : USA

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