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    Acella Pharmaceuticals

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    01 2AMIODARONE HYDROCHLORIDE

    02 2BENZONATATE

    03 1BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

    04 1CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE

    05 1CICLOPIROX

    06 1DOXYCYCLINE HYCLATE

    07 1DUTASTERIDE

    08 1GABAPENTIN

    09 1LACOSAMIDE

    10 1MEPROBAMATE

    11 1NIFEDIPINE

    12 1PHENYTOIN SODIUM

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    01

    Brand Name : AMIODARONE HYDROCHLO...

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    Brand Name : AMIODARONE HYDROCHLO...

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    RLD : No

    TE Code : AP

    AMIODARONE HYDROCHLORIDE

    Acella Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : AMIODARONE HYDROCHLORIDE

    Dosage Strength : 50MG/ML

    Approval Date : 2008-10-30

    Application Number : 77610

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    02

    Brand Name : AMIODARONE HYDROCHLO...

    U.S.A
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    Brand Name : AMIODARONE HYDROCHLO...

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    RLD : No

    TE Code : AP

    AMIODARONE HYDROCHLORIDE

    Acella Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : AMIODARONE HYDROCHLORIDE

    Dosage Strength : 50MG/ML

    Approval Date : 2008-10-30

    Application Number : 77834

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    Brand Name : BENZONATATE

    U.S.A
    AAPS
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    Brand Name : BENZONATATE

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    RLD : No

    TE Code :

    BENZONATATE

    Acella Pharmaceuticals

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : BENZONATATE

    Dosage Strength : 100MG

    Approval Date : 2015-01-16

    Application Number : 91310

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    Brand Name : BENZONATATE

    U.S.A
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    RLD : No

    TE Code :

    BENZONATATE

    Acella Pharmaceuticals

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : BENZONATATE

    Dosage Strength : 200MG

    Approval Date : 2015-01-16

    Application Number : 91310

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : BROMPHENIRAMINE MALE...

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    Brand Name : BROMPHENIRAMINE MALE...

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    RLD : No

    TE Code : AA

    BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE

    Acella Pharmaceuticals

    Dosage Form : SYRUP; ORAL

    Proprietary Name : BROMPHENIRAMINE MALEATE,...

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

    Approval Date : 2016-09-20

    Application Number : 203375

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    06

    Brand Name : HYDROCODONE BITARTRA...

    U.S.A
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    Brand Name : HYDROCODONE BITARTRA...

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    RLD : No

    TE Code :

    CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE

    Acella Pharmaceuticals

    Dosage Form : SOLUTION; ORAL

    Proprietary Name : HYDROCODONE BITARTRATE A...

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

    Approval Date : 2017-06-09

    Application Number : 206891

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : CICLOPIROX

    U.S.A
    AAPS
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    Brand Name : CICLOPIROX

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    RLD : No

    TE Code : AT

    CICLOPIROX

    Acella Pharmaceuticals

    Dosage Form : SOLUTION; TOPICAL

    Proprietary Name : CICLOPIROX

    Dosage Strength : 8%

    Approval Date : 2007-09-18

    Application Number : 78172

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AT

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    08

    Brand Name : DOXYCYCLINE HYCLATE

    U.S.A
    AAPS
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    Brand Name : DOXYCYCLINE HYCLATE

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    RLD : No

    TE Code : AB

    DOXYCYCLINE HYCLATE

    Acella Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : DOXYCYCLINE HYCLATE

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2020-03-16

    Application Number : 210664

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : DUTASTERIDE

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : DUTASTERIDE

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    RLD : No

    TE Code : AB

    DUTASTERIDE

    Acella Pharmaceuticals

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : DUTASTERIDE

    Dosage Strength : 0.5MG

    Approval Date : 2016-03-17

    Application Number : 206373

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    Brand Name : GABAPENTIN

    U.S.A
    AAPS
    Not Confirmed
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    Brand Name : GABAPENTIN

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    RLD : No

    TE Code : AA

    GABAPENTIN

    Acella Pharmaceuticals

    Dosage Form : SOLUTION; ORAL

    Proprietary Name : GABAPENTIN

    Dosage Strength : 250MG/5ML

    Approval Date : 2012-05-01

    Application Number : 76403

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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