FDA Approved Drugs Database

HANFORD GC

  • Drug Name:

    AMPICILLIN SODIUM

  • Application Number:

    63147

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE;INJECTION

  • Strength:

    EQ 500MG BASE/VIAL

  • Product Type:

  • Active Ingredient:

    AMPICILLIN SODIUM

  • Approval Date:

  • Legal Name:

    -

HEYL CHEMISCH

  • Drug Name:

    RADIOGARDASE (PRUSSIAN BLUE)

  • Application Number:

    21626

  • Product Number:

    1

  • Dosage Form:

    CAPSULE;ORAL

  • Strength:

    500MG

  • Product Type:

    RX

  • Active Ingredient:

    FERRIC HEXACYANOFERRATE(II)

  • Approval Date:

    2003-10-02

  • Legal Name:

    -

HOPE PHARMS

+2

  • Drug Name:

    SODIUM THIOSULFATE

  • Application Number:

    203923

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;INTRAVENOUS

  • Strength:

    12.5GM/50ML (250MG/ML)

  • Product Type:

    RX

  • Active Ingredient:

    SODIUM THIOSULFATE

  • Approval Date:

    2012-02-14

  • Legal Name:

    -

HQ SPCLT PHARMA

+36

  • Drug Name:

    DILTIAZEM HYDROCHLORIDE IN 0.72% SODIUM CHLORIDE

  • Application Number:

    218038

  • Product Number:

    2

  • Dosage Form:

    SOLUTION;INTRAVENOUS

  • Strength:

    250MG/250ML (1MG/ML)

  • Product Type:

    RX

  • Active Ingredient:

    DILTIAZEM HYDROCHLORIDE

  • Approval Date:

    2025-02-21

  • Legal Name:

    -

HQ SPECLT PHARMA

+15

  • Drug Name:

    AMPICILLIN AND SULBACTAM

  • Application Number:

    65188

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE;INJECTION

  • Strength:

    EQ 10GM BASE/VIAL;EQ 5GM BASE/VIAL

  • Product Type:

    RX

  • Active Ingredient:

    AMPICILLIN SODIUM; SULBACTAM SODIUM

  • Approval Date:

    2005-11-25

  • Legal Name:

    -

INDICUS PHARMA

+6

  • Drug Name:

    LETROZOLE

  • Application Number:

    201804

  • Product Number:

    1

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    2.5MG

  • Product Type:

    DISCN

  • Active Ingredient:

    LETROZOLE

  • Approval Date:

    2011-06-03

  • Legal Name:

    -

INSIGHT PHARMS

+1

  • Drug Name:

    MONISTAT-DERM

  • Application Number:

    17739

  • Product Number:

    1

  • Dosage Form:

    LOTION;TOPICAL

  • Strength:

    2%

  • Product Type:

    DISCN

  • Active Ingredient:

    MICONAZOLE NITRATE

  • Approval Date:

    1982-01-01

  • Legal Name:

    -

Avet Pharmaceuticals

+13

  • Drug Name:

    DUTASTERIDE

  • Application Number:

    207935

  • Product Number:

    1

  • Dosage Form:

    CAPSULE;ORAL

  • Strength:

    0.5MG

  • Product Type:

    DISCN

  • Active Ingredient:

    DUTASTERIDE

  • Approval Date:

    2017-10-13

  • Legal Name:

    -

GUERBET

+15

  • Drug Name:

    ELUCIREM

  • Application Number:

    216986

  • Product Number:

    7

  • Dosage Form:

    SOLUTION;INTRAVENOUS

  • Strength:

    48.51GM/100ML (485.1MG/ML)

  • Product Type:

    RX

  • Active Ingredient:

    GADOPICLENOL

  • Approval Date:

    2022-09-21

  • Legal Name:

    -

HRA Pharma

  • Drug Name:

    ELLA

  • Application Number:

    22474

  • Product Number:

    1

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    30MG

  • Product Type:

    RX

  • Active Ingredient:

    ULIPRISTAL ACETATE

  • Approval Date:

    2010-08-13

  • Legal Name:

    -

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