FDA Approved Drugs Database

Sunshine Lake Pharma Co., Ltd.

+76

  • Drug Name:

    LANGLARA

  • Application Number:

    761412

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE;SUBCUTANEOUS

  • Strength:

    100UNITS/ML

  • Product Type:

  • Active Ingredient:

    INSULIN GLARGINE-ALDY

  • Approval Date:

  • Legal Name:

    -

Tedor Pharma Inc.

+1

  • Drug Name:

    BENZPHETAMINE HYDROCHLORIDE

  • Application Number:

    40747

  • Product Number:

    2

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    25MG

  • Product Type:

    DISCN

  • Active Ingredient:

    BENZPHETAMINE HYDROCHLORIDE

  • Approval Date:

    2015-11-20

  • Legal Name:

    -

Sterling Spa

  • Drug Name:

    BRONKAID MIST

  • Application Number:

    16803

  • Product Number:

    1

  • Dosage Form:

    AEROSOL, METERED;INHALATION

  • Strength:

    0.25MG/INH

  • Product Type:

    DISCN

  • Active Ingredient:

    EPINEPHRINE

  • Approval Date:

    1982-01-01

  • Legal Name:

    -

Sun Pharmaceutical Industries Limited

+1030

  • Drug Name:

    ILUMYA

  • Application Number:

    761067

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE;INJECTION

  • Strength:

    100MG/1ML

  • Product Type:

  • Active Ingredient:

    TILDRAKIZUMAB-ASMN

  • Approval Date:

  • Legal Name:

    -

Synthon Pharmaceuticals

+31

  • Drug Name:

    OZANIMOD

  • Application Number:

    219236

  • Product Number:

    3

  • Dosage Form:

    CAPSULE

  • Strength:

    0.23MG

  • Product Type:

  • Active Ingredient:

    OZANIMOD

  • Approval Date:

  • Legal Name:

    -

Taro Pharmaceutical Industries

+208

  • Drug Name:

    LAMOTRIGINE

  • Application Number:

    219677

  • Product Number:

    4

  • Dosage Form:

    TABLET, ORALLY DISINTEGRATING;ORAL

  • Strength:

    200MG

  • Product Type:

    RX

  • Active Ingredient:

    LAMOTRIGINE

  • Approval Date:

    2025-10-07

  • Legal Name:

    -

Teva Pharmaceutical Industries

+830

  • Drug Name:

    AJOVY

  • Application Number:

    761089

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE;INJECTION

  • Strength:

    150MG/ML

  • Product Type:

  • Active Ingredient:

    FREMANEZUMAB-VFRM

  • Approval Date:

  • Legal Name:

    -

The Ritedose Corporation

+10

  • Drug Name:

    ALBUTEROL SULFATE

  • Application Number:

    218386

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;INHALATION

  • Strength:

    EQ 0.5% BASE

  • Product Type:

    RX

  • Active Ingredient:

    ALBUTEROL SULFATE

  • Approval Date:

    2025-03-12

  • Legal Name:

    -

Tianjin Tianyao Pharmaceuticals Co., Ltd.

+9

  • Drug Name:

    METHYLPREDNISOLONE SODIUM SUCCINATE

  • Application Number:

    212396

  • Product Number:

    5

  • Dosage Form:

    INJECTABLE;INJECTION

  • Strength:

    EQ 2GM BASE/VIAL

  • Product Type:

    RX

  • Active Ingredient:

    METHYLPREDNISOLONE SODIUM SUCCINATE

  • Approval Date:

    2021-04-20

  • Legal Name:

    -

Tolmar

+14

  • Drug Name:

    FENSOLVI KIT

  • Application Number:

    213150

  • Product Number:

    1

  • Dosage Form:

    POWDER;SUBCUTANEOUS

  • Strength:

    45MG

  • Product Type:

    RX

  • Active Ingredient:

    LEUPROLIDE ACETATE

  • Approval Date:

    2020-05-01

  • Legal Name:

    -

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