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    Acella Pharmaceuticals

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    01 2AMIODARONE HYDROCHLORIDE

    02 2BENZONATATE

    03 1BETAXOLOL HYDROCHLORIDE

    04 1BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

    05 1CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE

    06 1CICLOPIROX

    07 1DOXYCYCLINE HYCLATE

    08 1DUTASTERIDE

    09 1GABAPENTIN

    10 1LACOSAMIDE

    11 1MEPROBAMATE

    12 1NIFEDIPINE

    13 1PHENYTOIN SODIUM

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    01

    Brand Name : AMIODARONE HYDROCHLO...

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    Brand Name : AMIODARONE HYDROCHLO...

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    Regulatory Info : RX

    Registration Country : USA

    AMIODARONE HYDROCHLORIDE

    Acella Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : AMIODARONE HYDROCHLORIDE

    Dosage Strength : 50MG/ML

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    Approval Date : 2008-10-30

    Application Number : 77610

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : AMIODARONE HYDROCHLO...

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    Regulatory Info : RX

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    AMIODARONE HYDROCHLORIDE

    Acella Pharmaceuticals

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : AMIODARONE HYDROCHLORIDE

    Dosage Strength : 50MG/ML

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    Approval Date : 2008-10-30

    Application Number : 77834

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : BENZONATATE

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    Regulatory Info : DISCN

    Registration Country : USA

    BENZONATATE

    Acella Pharmaceuticals

    Dosage Form : CAPSULE;ORAL

    Brand Name : BENZONATATE

    Dosage Strength : 100MG

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    Approval Date : 2015-01-16

    Application Number : 91310

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

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    BENZONATATE

    Acella Pharmaceuticals

    Dosage Form : CAPSULE;ORAL

    Brand Name : BENZONATATE

    Dosage Strength : 200MG

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    Approval Date : 2015-01-16

    Application Number : 91310

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Brand Name : BETAXOLOL HYDROCHLOR...

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    Regulatory Info : RX

    Registration Country : USA

    BETAXOLOL HYDROCHLORIDE

    Acella Pharmaceuticals

    Dosage Form : SOLUTION/DROPS;OPHTHALMI...

    Brand Name : BETAXOLOL HYDROCHLORIDE

    Dosage Strength : EQ 0.5% BASE

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    Approval Date : 2009-11-16

    Application Number : 78694

    Regulatory Info : RX

    Registration Country : USA

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    06

    Brand Name : BROMPHENIRAMINE MALE...

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    Regulatory Info : RX

    Registration Country : USA

    BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

    Acella Pharmaceuticals

    Dosage Form : SYRUP;ORAL

    Brand Name : BROMPHENIRAMINE MALEATE, ...

    Dosage Strength : 2MG/5ML;10MG/5ML;30MG/...

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    Approval Date : 2016-09-20

    Application Number : 203375

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : HYDROCODONE BITARTRA...

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    Regulatory Info : DISCN

    Registration Country : USA

    CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE

    Acella Pharmaceuticals

    Dosage Form : SOLUTION;ORAL

    Brand Name : HYDROCODONE BITARTRATE AN...

    Dosage Strength : 4MG/5ML;5MG/5ML

    Packaging :

    Approval Date : 2017-06-09

    Application Number : 206891

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Brand Name : CICLOPIROX

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    Brand Name : CICLOPIROX

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    Regulatory Info : RX

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    CICLOPIROX

    Acella Pharmaceuticals

    Dosage Form : SOLUTION;TOPICAL

    Brand Name : CICLOPIROX

    Dosage Strength : 8%

    Packaging :

    Approval Date : 2007-09-18

    Application Number : 78172

    Regulatory Info : RX

    Registration Country : USA

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    09

    Brand Name : DOXYCYCLINE HYCLATE

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    Brand Name : DOXYCYCLINE HYCLATE

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    Regulatory Info : RX

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    DOXYCYCLINE HYCLATE

    Acella Pharmaceuticals

    Dosage Form : TABLET;ORAL

    Brand Name : DOXYCYCLINE HYCLATE

    Dosage Strength : EQ 100MG BASE

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    Approval Date : 2020-03-16

    Application Number : 210664

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : DUTASTERIDE

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    DUTASTERIDE

    Acella Pharmaceuticals

    Dosage Form : CAPSULE;ORAL

    Brand Name : DUTASTERIDE

    Dosage Strength : 0.5MG

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    Approval Date : 2016-03-17

    Application Number : 206373

    Regulatory Info : RX

    Registration Country : USA

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