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    Johnson & Johnson Innovative Medicine

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    01 4ACETAMINOPHEN; CODEINE PHOSPHATE

    02 1ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE

    03 1ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE

    04 2ALMOTRIPTAN MALATE

    05 2BEDAQUILINE FUMARATE

    06 3BOSENTAN

    07 2CANAGLIFLOZIN

    08 8CANAGLIFLOZIN; METFORMIN HYDROCHLORIDE

    09 1CHLORZOXAZONE

    10 4CISAPRIDE MONOHYDRATE

    11 1CLADRIBINE

    12 3COBICISTAT; DARUNAVIR ETHANOLATE

    13 1COBICISTAT; DARUNAVIR; EMTRICITABINE; TENOFOVIR ALAFENAMIDE FUMARATE

    14 2CYCLOBENZAPRINE HYDROCHLORIDE

    15 7DARUNAVIR

    16 2DARUNAVIR AND COBICISTAT

    17 2DESOGESTREL; ETHINYL ESTRADIOL

    18 2EPOPROSTENOL SODIUM

    19 1ESKETAMINE HYDROCHLORIDE

    20 1ETHINYL ESTRADIOL; NORELGESTROMIN

    21 4ETHINYL ESTRADIOL; NORETHINDRONE

    22 5ETHINYL ESTRADIOL; NORGESTIMATE

    23 3ETRAVIRINE

    24 6FENTANYL

    25 7GALANTAMINE HYDROBROMIDE

    26 2HALOPERIDOL DECANOATE

    27 1HALOPERIDOL LACTATE

    28 3ILOPROST

    29 4ITRACONAZOLE

    30 4KETOCONAZOLE

    31 1LEVAMISOLE HYDROCHLORIDE

    32 9LEVOFLOXACIN

    33 1LOPERAMIDE HYDROCHLORIDE

    34 1MACITENTAN

    35 2MACITENTAN; TADALAFIL

    36 2MEBENDAZOLE

    37 4METHYLPHENIDATE HYDROCHLORIDE

    38 1MICONAZOLE

    39 1MIGLUSTAT

    40 1NORETHINDRONE

    41 3OFLOXACIN

    42 4OXYBUTYNIN CHLORIDE

    43 9PALIPERIDONE

    44 11PALIPERIDONE PALMITATE

    45 1PENTOSAN POLYSULFATE SODIUM

    46 2RILPIVIRINE HYDROCHLORIDE

    47 17RISPERIDONE

    48 9RIVAROXABAN

    49 9SELEXIPAG

    50 1SIMEPREVIR SODIUM

    51 3TERCONAZOLE

    52 9TOPIRAMATE

    53 1TRABECTEDIN

    54 2TRAMADOL HYDROCHLORIDE

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    01

    Brand Name : TYLENOL W/ CODEINE N...

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Brand Name : TYLENOL W/ CODEINE N...

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    RLD : No

    TE Code :

    ACETAMINOPHEN; CODEINE PHOSPHATE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : TYLENOL W/ CODEINE NO. 1

    Dosage Strength : 300MG;7.5MG

    Approval Date : 1982-01-01

    Application Number : 85055

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : TYLENOL W/ CODEINE N...

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
    arrow

    Brand Name : TYLENOL W/ CODEINE N...

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    ACETAMINOPHEN; CODEINE PHOSPHATE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : TYLENOL W/ CODEINE NO. 2

    Dosage Strength : 300MG;15MG

    Approval Date : 1982-01-01

    Application Number : 85055

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    03

    Brand Name : TYLENOL W/ CODEINE N...

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Brand Name : TYLENOL W/ CODEINE N...

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    RLD : Yes

    TE Code :

    ACETAMINOPHEN; CODEINE PHOSPHATE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : TYLENOL W/ CODEINE NO. 3

    Dosage Strength : 300MG;30MG

    Approval Date : 1982-01-01

    Application Number : 85055

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    04

    Brand Name : TYLENOL W/ CODEINE N...

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Brand Name : TYLENOL W/ CODEINE N...

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    RLD : Yes

    TE Code :

    ACETAMINOPHEN; CODEINE PHOSPHATE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : TYLENOL W/ CODEINE NO. 4

    Dosage Strength : 300MG;60MG

    Approval Date : 1982-01-01

    Application Number : 85055

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    05

    Brand Name : TYLOX

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    06

    Brand Name : ULTRACET

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Brand Name : ULTRACET

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    RLD : Yes

    TE Code :

    ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : ULTRACET

    Dosage Strength : 325MG;37.5MG **Federal R...

    Approval Date : 2001-08-15

    Application Number : 21123

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    07

    Brand Name : AXERT

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Brand Name : AXERT

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    RLD : Yes

    TE Code :

    ALMOTRIPTAN MALATE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : AXERT

    Dosage Strength : EQ 6.25MG BASE **Federal...

    Approval Date : 2001-05-07

    Application Number : 21001

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    08

    Brand Name : AXERT

    U.S.A
    AMWC Asia-TDAC
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    Brand Name : AXERT

    U.S.A
    AMWC Asia-TDAC
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    RLD : Yes

    TE Code :

    ALMOTRIPTAN MALATE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : AXERT

    Dosage Strength : EQ 12.5MG BASE **Federal...

    Approval Date : 2001-05-07

    Application Number : 21001

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    09

    Brand Name : SIRTURO

    U.S.A
    AMWC Asia-TDAC
    Not Confirmed
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    Brand Name : SIRTURO

    U.S.A
    AMWC Asia-TDAC
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    RLD : Yes

    TE Code :

    BEDAQUILINE FUMARATE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : SIRTURO

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2012-12-28

    Application Number : 204384

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    10

    Brand Name : SIRTURO

    U.S.A
    AMWC Asia-TDAC
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    Brand Name : SIRTURO

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    RLD : Yes

    TE Code :

    BEDAQUILINE FUMARATE

    Johnson & Johnson Innovative Medicine

    Dosage Form : TABLET; ORAL

    Proprietary Name : SIRTURO

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2020-05-27

    Application Number : 204384

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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