FDA Approved Drugs Database

CLONMEL HLTHCARE

+1

  • Drug Name:

    METHOCARBAMOL

  • Application Number:

    85963

  • Product Number:

    1

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    750MG

  • Product Type:

    DISCN

  • Active Ingredient:

    METHOCARBAMOL

  • Approval Date:

    1982-01-01

  • Legal Name:

    -

COASTAL PHARMS

  • Drug Name:

    BROMFENAC SODIUM

  • Application Number:

    201211

  • Product Number:

    1

  • Dosage Form:

    SOLUTION/DROPS;OPHTHALMIC

  • Strength:

    EQ 0.09% ACID

  • Product Type:

    DISCN

  • Active Ingredient:

    BROMFENAC SODIUM

  • Approval Date:

    2011-05-11

  • Legal Name:

    -

CONCORDIA PHARMS INC

+4

  • Drug Name:

    ORAPRED

  • Application Number:

    75117

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;ORAL

  • Strength:

    EQ 15MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

  • Product Type:

    DISCN

  • Active Ingredient:

    PREDNISOLONE SODIUM PHOSPHATE

  • Approval Date:

    2000-12-14

  • Legal Name:

    -

CUBIST PHARMS INC

  • Drug Name:

    ENTEREG

  • Application Number:

    21775

  • Product Number:

    1

  • Dosage Form:

    CAPSULE;ORAL

  • Strength:

    12MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

  • Product Type:

    DISCN

  • Active Ingredient:

    ALVIMOPAN

  • Approval Date:

    2008-05-20

  • Legal Name:

    -

CYPRESS PHARM

+4

  • Drug Name:

    CARBINOXAMINE MALEATE

  • Application Number:

    90418

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;ORAL

  • Strength:

    4MG/5ML

  • Product Type:

    DISCN

  • Active Ingredient:

    CARBINOXAMINE MALEATE

  • Approval Date:

    2010-05-04

  • Legal Name:

    -

DANCO LABS LLC

  • Drug Name:

    MIFEPREX

  • Application Number:

    20687

  • Product Number:

    1

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    200MG

  • Product Type:

    RX

  • Active Ingredient:

    MIFEPRISTONE

  • Approval Date:

    2000-09-28

  • Legal Name:

    -

DAVA PHARMS INC

+46

  • Drug Name:

    CHLORPROPAMIDE

  • Application Number:

    89562

  • Product Number:

    1

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    250MG

  • Product Type:

    DISCN

  • Active Ingredient:

    CHLORPROPAMIDE

  • Approval Date:

    1987-09-04

  • Legal Name:

    -

CPPI CV

+6

  • Drug Name:

    SUTENT

  • Application Number:

    21968

  • Product Number:

    3

  • Dosage Form:

    CAPSULE; ORAL

  • Strength:

    EQ 50MG BASE

  • Product Type:

  • Active Ingredient:

    SUNITINIB MALATE

  • Approval Date:

  • Legal Name:

    -

CUMBERLAND PHARMS

  • Drug Name:

    VAPRISOL

  • Application Number:

    22016

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE; INJECTION

  • Strength:

    20MG

  • Product Type:

  • Active Ingredient:

    CONIVAPTAN HYDROCHLORIDE

  • Approval Date:

  • Legal Name:

    -

DAITO CORP

  • Drug Name:

    METHOTREXATE SODIUM

  • Application Number:

    213362

  • Product Number:

    1

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    EQ 2.5MG BASE

  • Product Type:

    DISCN

  • Active Ingredient:

    METHOTREXATE SODIUM

  • Approval Date:

    2023-08-07

  • Legal Name:

    -

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