FDA Approved Drugs Database

Luitpold Pharmaceuticals, Inc.

+30

  • Drug Name:

    METOPROLOL TARTRATE

  • Application Number:

    91307

  • Product Number:

    1

  • Dosage Form:

    INJECTABLE;INJECTION

  • Strength:

    1MG/ML

  • Product Type:

    DISCN

  • Active Ingredient:

    METOPROLOL TARTRATE

  • Approval Date:

    2010-12-29

  • Legal Name:

    -

Lyne Laboratories, Inc.

+4

  • Drug Name:

    SODIUM POLYSTYRENE SULFONATE

  • Application Number:

    214912

  • Product Number:

    1

  • Dosage Form:

    SUSPENSION;ORAL, RECTAL

  • Strength:

    15GM/60ML

  • Product Type:

    RX

  • Active Ingredient:

    SODIUM POLYSTYRENE SULFONATE

  • Approval Date:

    2025-06-10

  • Legal Name:

    -

McGuff Pharmaceuticals Inc.

  • Drug Name:

    ASCOR

  • Application Number:

    209112

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;INTRAVENOUS

  • Strength:

    25,000MG/50ML (500MG/ML)

  • Product Type:

    RX

  • Active Ingredient:

    ASCORBIC ACID

  • Approval Date:

    2017-10-02

  • Legal Name:

    -

Medefil, Inc.

+12

  • Drug Name:

    ATROPINE SULFATE

  • Application Number:

    214970

  • Product Number:

    1

  • Dosage Form:

    SOLUTION;INTRAVENOUS

  • Strength:

    1MG/10ML (0.1MG/ML)

  • Product Type:

    RX

  • Active Ingredient:

    ATROPINE SULFATE

  • Approval Date:

    2022-11-04

  • Legal Name:

    -

Lupin Ltd

+583

  • Drug Name:

    RANLUSPEC

  • Application Number:

    761480

  • Product Number:

    2

  • Dosage Form:

    INJECTION

  • Strength:

    6MG/ML

  • Product Type:

  • Active Ingredient:

    RANIBIZUMAB-HKDZ

  • Approval Date:

  • Legal Name:

    -

Macleods Pharmaceuticals Limited

+426

  • Drug Name:

    MEXILETINE HYDROCHLORIDE

  • Application Number:

    219987

  • Product Number:

    3

  • Dosage Form:

    CAPSULE;ORAL

  • Strength:

    250MG

  • Product Type:

    RX

  • Active Ingredient:

    MEXILETINE HYDROCHLORIDE

  • Approval Date:

    2026-03-23

  • Legal Name:

    -

Mallinckrodt Pharmaceuticals

+243

  • Drug Name:

    TOFACITINIB CITRATE

  • Application Number:

    219395

  • Product Number:

    2

  • Dosage Form:

    TABLET;ORAL

  • Strength:

    EQ 10MG BASE

  • Product Type:

    RX

  • Active Ingredient:

    TOFACITINIB CITRATE

  • Approval Date:

    2026-06-03

  • Legal Name:

    -

Marksans Pharma

+37

  • Drug Name:

    BENZONATATE

  • Application Number:

    220298

  • Product Number:

    2

  • Dosage Form:

    CAPSULE;ORAL

  • Strength:

    200MG

  • Product Type:

    RX

  • Active Ingredient:

    BENZONATATE

  • Approval Date:

    2026-03-30

  • Legal Name:

    -

Meda Pharmaceuticals Inc.

+8

  • Drug Name:

    BUTISOL SODIUM

  • Application Number:

    85380

  • Product Number:

    1

  • Dosage Form:

    ELIXIR;ORAL

  • Strength:

    30MG/5ML

  • Product Type:

    DISCN

  • Active Ingredient:

    BUTABARBITAL SODIUM

  • Approval Date:

    1982-01-01

  • Legal Name:

    -

Merck & Co

+133

  • Drug Name:

    ELSPAR

  • Application Number:

    101063

  • Product Number:

    1

  • Dosage Form:

    VIAL

  • Strength:

    10,000IU/VIAL

  • Product Type:

  • Active Ingredient:

    ASPARAGINASE

  • Approval Date:

  • Legal Name:

    -

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