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    Somerset Pharmaceuticals Inc

    EVENTS

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    DIGITAL CONTENT

    DEVELOPMENTS

    FINISHED DOSAGE FORMULATIONS

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    01 3ACARBOSE

    02 3ACETYLCYSTEINE

    03 2AMINOCAPROIC ACID

    04 5ATROPINE SULFATE

    05 1AZELASTINE HYDROCHLORIDE

    06 1BEPOTASTINE BESILATE

    07 1BIMATOPROST

    08 2BRIMONIDINE TARTRATE

    09 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE

    10 2BUPIVACAINE HYDROCHLORIDE

    11 1BUPRENORPHINE HYDROCHLORIDE

    12 1CABERGOLINE

    13 1CALCIUM CHLORIDE

    14 2CALCIUM GLUCONATE

    15 3CISATRACURIUM BESYLATE

    16 1CLONIDINE HYDROCHLORIDE

    17 1CUPRIC CHLORIDE

    18 2CYANOCOBALAMIN

    19 3DEXAMETHASONE SODIUM PHOSPHATE

    20 2DEXMEDETOMIDINE HYDROCHLORIDE

    21 2DICYCLOMINE HYDROCHLORIDE

    22 1DIHYDROERGOTAMINE MESYLATE

    23 1DORZOLAMIDE HYDROCHLORIDE

    24 1DORZOLAMIDE HYDROCHLORIDE; TIMOLOL MALEATE

    25 3DROXIDOPA

    26 4ELTROMBOPAG OLAMINE

    27 1EPINASTINE HYDROCHLORIDE

    28 1GLYCOPYRROLATE

    29 2HALOPERIDOL DECANOATE

    30 3HYDROXYZINE HYDROCHLORIDE

    31 1ISOPROTERENOL HYDROCHLORIDE

    32 1ISOSULFAN BLUE

    33 1LACOSAMIDE

    34 1LATANOPROST

    35 2MEMANTINE HYDROCHLORIDE

    36 1METHOCARBAMOL

    37 1MOXIFLOXACIN HYDROCHLORIDE

    38 4NALBUPHINE HYDROCHLORIDE

    39 2NALOXONE HYDROCHLORIDE

    40 2OFLOXACIN

    41 2OLOPATADINE HYDROCHLORIDE

    42 1PHENYLEPHRINE HYDROCHLORIDE

    43 3PILOCARPINE HYDROCHLORIDE

    44 1POLYMYXIN B SULFATE; TRIMETHOPRIM SULFATE

    45 2POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM PHOSPHATE, MONOBASIC

    46 6PREGABALIN

    47 1PROCHLORPERAZINE EDISYLATE

    48 1PROPARACAINE HYDROCHLORIDE

    49 2PRUCALOPRIDE SUCCINATE

    50 1RILPIVIRINE

    51 7ROPIVACAINE HYDROCHLORIDE

    52 6SELEGILINE

    53 2SODIUM ACETATE

    54 1SODIUM NITROPRUSSIDE

    55 1SUCCINYLCHOLINE CHLORIDE

    56 1SULFAMETHOXAZOLE; TRIMETHOPRIM

    57 2TERIFLUNOMIDE

    58 1TETRACAINE HYDROCHLORIDE

    59 1TIMOLOL

    60 5TIMOLOL MALEATE

    61 1TOBRAMYCIN

    62 1TRAVOPROST

    63 1TROPICAMIDE

    64 1VALGANCICLOVIR HYDROCHLORIDE

    65 4VALSARTAN

    66 4VERAPAMIL HYDROCHLORIDE

    67 1ZINC CHLORIDE

    68 2ZINC SULFATE

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    01

    Brand Name : ACARBOSE

    U.S.A
    DDL Conference
    Not Confirmed
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    Brand Name : ACARBOSE

    U.S.A
    DDL Conference
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    Digital Content Digital Content

    RLD : No

    TE Code : AB

    ACARBOSE

    Somerset Pharmaceuticals Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : ACARBOSE

    Dosage Strength : 25MG

    Approval Date : 2013-10-17

    Application Number : 91343

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    Brand Name : ACARBOSE

    U.S.A
    DDL Conference
    Not Confirmed
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    Brand Name : ACARBOSE

    U.S.A
    DDL Conference
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    RLD : No

    TE Code : AB

    ACARBOSE

    Somerset Pharmaceuticals Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : ACARBOSE

    Dosage Strength : 50MG

    Approval Date : 2013-10-17

    Application Number : 91343

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    Brand Name : ACARBOSE

    U.S.A
    DDL Conference
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    Brand Name : ACARBOSE

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    RLD : No

    TE Code : AB

    ACARBOSE

    Somerset Pharmaceuticals Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : ACARBOSE

    Dosage Strength : 100MG

    Approval Date : 2013-10-17

    Application Number : 91343

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : ACETYLCYSTEINE

    U.S.A
    DDL Conference
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    Brand Name : ACETYLCYSTEINE

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    RLD : No

    TE Code : AP

    ACETYLCYSTEINE

    Somerset Pharmaceuticals Inc

    Dosage Form : INJECTABLE; INTRAVENOUS

    Proprietary Name : ACETYLCYSTEINE

    Dosage Strength : 6GM/30ML (200MG/ML)

    Approval Date : 2024-06-07

    Application Number : 218397

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    05

    Brand Name : ACETYLCYSTEINE

    U.S.A
    DDL Conference
    Not Confirmed
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    Brand Name : ACETYLCYSTEINE

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    RLD : No

    TE Code : AN

    ACETYLCYSTEINE

    Somerset Pharmaceuticals Inc

    Dosage Form : SOLUTION; INHALATION, ORAL

    Proprietary Name : ACETYLCYSTEINE

    Dosage Strength : 10%

    Approval Date : 2025-02-12

    Application Number : 219194

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    06

    Brand Name : ACETYLCYSTEINE

    U.S.A
    DDL Conference
    Not Confirmed
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    Brand Name : ACETYLCYSTEINE

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    DDL Conference
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    RLD : No

    TE Code : AN

    ACETYLCYSTEINE

    Somerset Pharmaceuticals Inc

    Dosage Form : SOLUTION; INHALATION, ORAL

    Proprietary Name : ACETYLCYSTEINE

    Dosage Strength : 20%

    Approval Date : 2025-02-12

    Application Number : 219194

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    07

    Brand Name : AMINOCAPROIC ACID

    U.S.A
    DDL Conference
    Not Confirmed
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    Brand Name : AMINOCAPROIC ACID

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    DDL Conference
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    RLD : No

    TE Code : AB

    AMINOCAPROIC ACID

    Somerset Pharmaceuticals Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMINOCAPROIC ACID

    Dosage Strength : 500MG

    Approval Date : 2022-09-14

    Application Number : 213944

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    Brand Name : AMINOCAPROIC ACID

    U.S.A
    DDL Conference
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    Brand Name : AMINOCAPROIC ACID

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    DDL Conference
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    RLD : No

    TE Code : AB

    AMINOCAPROIC ACID

    Somerset Pharmaceuticals Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : AMINOCAPROIC ACID

    Dosage Strength : 1GM

    Approval Date : 2022-09-14

    Application Number : 213944

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : ATROPINE SULFATE

    U.S.A
    DDL Conference
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    Brand Name : ATROPINE SULFATE

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    RLD : No

    TE Code : AP

    ATROPINE SULFATE

    Somerset Pharmaceuticals Inc

    Dosage Form : SOLUTION; INTRAVENOUS, INTRAMU...

    Proprietary Name : ATROPINE SULFATE

    Dosage Strength : 8MG/20ML (0.4MG/ML)

    Approval Date : 2024-11-29

    Application Number : 215005

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    10

    Brand Name : ATROPINE SULFATE

    U.S.A
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    Brand Name : ATROPINE SULFATE

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    RLD : No

    TE Code : AT2

    ATROPINE SULFATE

    Somerset Pharmaceuticals Inc

    Dosage Form : SOLUTION/DROPS; OPHTHALMIC

    Proprietary Name : ATROPINE SULFATE

    Dosage Strength : 1%

    Approval Date : 2024-04-29

    Application Number : 217791

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AT2

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