FDA Approved Drugs Database

Elite Laboratories, Inc.

+59

  • Drug Name:

    LISDEXAMFETAMINE DIMESYLATE

  • Application Number:

    218604

  • Product Number:

    7

  • Dosage Form:

    CAPSULE;ORAL

  • Strength:

    70MG

  • Product Type:

    RX

  • Active Ingredient:

    LISDEXAMFETAMINE DIMESYLATE

  • Approval Date:

    2024-11-15

  • Legal Name:

    -

Exela Pharma Sciences, LLC.

  • Drug Name:

    CAFFEINE CITRATE

  • Application Number:

    77233

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;INTRAVENOUS

  • Strength:

    EQ 30MG BASE/3ML (EQ 10MG BASE/ML)

  • Product Type:

    RX

  • Active Ingredient:

    CAFFEINE CITRATE

  • Approval Date:

    2006-09-21

  • Legal Name:

    -

Douglas CDMO

  • Drug Name:

    VERSACLOZ

  • Application Number:

    203479

  • Product Number:

    1

  • Dosage Form:

    SUSPENSION;ORAL

  • Strength:

    50MG/ML

  • Product Type:

    RX

  • Active Ingredient:

    CLOZAPINE

  • Approval Date:

    2013-02-06

  • Legal Name:

    -

Egis Pharmaceuticals PLC

+4

  • Drug Name:

    BUSPIRONE HYDROCHLORIDE

  • Application Number:

    75119

  • Product Number:

    3

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    15MG

  • Product Type:

    DISCN

  • Active Ingredient:

    BUSPIRONE HYDROCHLORIDE

  • Approval Date:

    2003-01-23

  • Legal Name:

    -

Emcure Pharmaceuticals

+22

  • Drug Name:

    DOLUTEGRAVIR AND LAMIVUDINE

  • Application Number:

    219623

  • Product Number:

    2

  • Dosage Form:

    TABLET

  • Strength:

    300MG

  • Product Type:

  • Active Ingredient:

    DOLUTEGRAVIR AND LAMIVUDINE

  • Approval Date:

  • Legal Name:

    -

EMD Millipore Corporation

+26

  • Drug Name:

    BAVENCIO

  • Application Number:

    761078

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE;INTRAVENOUS

  • Strength:

    20MG/ML

  • Product Type:

  • Active Ingredient:

    AVELUMAB

  • Approval Date:

  • Legal Name:

    -

Epic Pharma. LLC.

+359

  • Drug Name:

    OXCARBAZEPINE

  • Application Number:

    219556

  • Product Number:

    3

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    600MG

  • Product Type:

    RX

  • Active Ingredient:

    OXCARBAZEPINE

  • Approval Date:

    2026-03-02

  • Legal Name:

    -

Ethypharm

+7

  • Drug Name:

    BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE

  • Application Number:

    204431

  • Product Number:

    2

  • Dosage Form:

    TABLET;SUBLINGUAL

  • Strength:

    EQ 8MG BASE;EQ 2MG BASE

  • Product Type:

    RX

  • Active Ingredient:

    BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE

  • Approval Date:

    2015-10-16

  • Legal Name:

    -

FDC

+20

  • Drug Name:

    MOXIFLOXACIN HYDROCHLORIDE

  • Application Number:

    219475

  • Product Number:

    1

  • Dosage Form:

    SOLUTION/DROPS;OPHTHALMIC

  • Strength:

    EQ 0.5% BASE

  • Product Type:

    DISCN

  • Active Ingredient:

    MOXIFLOXACIN HYDROCHLORIDE

  • Approval Date:

    2025-08-04

  • Legal Name:

    -

Ferring Pharmaceuticals

+41

  • Drug Name:

    CLENPIQ

  • Application Number:

    209589

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;ORAL

  • Strength:

    12GM/BOT;3.5GM/BOT;10MG/BOT

  • Product Type:

    RX

  • Active Ingredient:

    CITRIC ACID; MAGNESIUM OXIDE; SODIUM PICOSULFATE

  • Approval Date:

    2017-11-28

  • Legal Name:

    -

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