FDA Approved Drugs Database

China Resources Saike Pharmaceutical Co., Ltd.

+4

  • Drug Name:

    LEVETIRACETAM

  • Application Number:

    205102

  • Product Number:

    4

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    500MG

  • Product Type:

    DISCN

  • Active Ingredient:

    LEVETIRACETAM

  • Approval Date:

    2015-12-16

  • Legal Name:

    -

Alvogen

+132

  • Drug Name:

    NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS)

  • Application Number:

    215002

  • Product Number:

    1

  • Dosage Form:

    CAPSULE;ORAL

  • Strength:

    75MG;25MG

  • Product Type:

    DISCN

  • Active Ingredient:

    NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE

  • Approval Date:

    2022-07-20

  • Legal Name:

    -

Aspen API

+9

  • Drug Name:

    ENJUVIA

  • Application Number:

    21443

  • Product Number:

    5

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    0.9MG

  • Product Type:

    DISCN

  • Active Ingredient:

    ESTROGENS, CONJUGATED SYNTHETIC B

  • Approval Date:

    2007-04-27

  • Legal Name:

    -

Astellas Pharma

+6

  • Drug Name:

    MYCAMINE

  • Application Number:

    21754

  • Product Number:

    2

  • Dosage Form:

    INJECTABLE; INJECTION

  • Strength:

    50MG

  • Product Type:

  • Active Ingredient:

    MICAFUNGIN SODIUM

  • Approval Date:

  • Legal Name:

    -

BASF

+5

  • Drug Name:

    IBU

  • Application Number:

    70745

  • Product Number:

    1

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    800MG

  • Product Type:

    DISCN

  • Active Ingredient:

    IBUPROFEN

  • Approval Date:

    1986-07-23

  • Legal Name:

    -

Breckenridge Pharmaceutical

+8

  • Drug Name:

    ESTRADIOL AND NORETHINDRONE ACETATE

  • Application Number:

    78324

  • Product Number:

    2

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    0.5MG;0.1MG

  • Product Type:

    RX

  • Active Ingredient:

    ESTRADIOL; NORETHINDRONE ACETATE

  • Approval Date:

    2011-06-09

  • Legal Name:

    -

Bristol Myers Squibb

+216

  • Drug Name:

    OPDUALAG

  • Application Number:

    761234

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;INTRAVENOUS

  • Strength:

    240MG;80MG

  • Product Type:

  • Active Ingredient:

    NIVOLUMAB;RELATLIMAB-RMBW

  • Approval Date:

  • Legal Name:

    -

Cardinal Health

+5

  • Drug Name:

    SODIUM FLUORIDE F-18

  • Application Number:

    203780

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE;INTRAVENOUS

  • Strength:

    10-200mCi/ML

  • Product Type:

    RX

  • Active Ingredient:

    SODIUM FLUORIDE F-18

  • Approval Date:

    2015-07-30

  • Legal Name:

    -

CordenPharma

+11

  • Drug Name:

    CEFZIL

  • Application Number:

    50665

  • Product Number:

    2

  • Dosage Form:

    FOR SUSPENSION;ORAL

  • Strength:

    250MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

  • Product Type:

    DISCN

  • Active Ingredient:

    CEFPROZIL

  • Approval Date:

    1991-12-23

  • Legal Name:

    -

Wyeth Pharmaceuticals Inc

+72

  • Drug Name:

    MYLOTARG

  • Application Number:

    761060

  • Product Number:

    1

  • Dosage Form:

    VIAL;SINGLE-DOSE

  • Strength:

    4.5MG

  • Product Type:

  • Active Ingredient:

    GEMTUZUMAB OZOGAMICIN

  • Approval Date:

  • Legal Name:

    -

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