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    BEDFORD LABS

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    MIDAZOLAM HYDROCHLORIDE

    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-23

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    MIDAZOLAM HYDROCHLORIDE

    Brand Name : VERSED

    Dosage Form : SYRUP;ORAL

    Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1998-10-15

    Application Number : 20942

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    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75154

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    Dosage Strength : EQ 1MG BASE/ML

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    Hikma Pharmaceuticals

    United Kingdom
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    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75243

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    Hikma Pharmaceuticals

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    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Application Number : 75243

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    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-23

    Application Number : 75247

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    Hikma Pharmaceuticals

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    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML

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    Application Number : 75247

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    09

    Hikma Pharmaceuticals

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    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75324

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    Hikma Pharmaceuticals

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    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75324

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    Hikma Pharmaceuticals

    United Kingdom
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    MIDAZOLAM HYDROCHLORIDE

    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75421

    Regulatory Info : RX

    Registration Country : USA

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    12

    Hospira, Inc.

    U.S.A
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    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75293

    Regulatory Info : RX

    Registration Country : USA

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    13

    Hospira, Inc.

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    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-20

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    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML

    Packaging :

    Approval Date : 2000-06-20

    Application Number : 75396

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    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75396

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    Registration Country : USA

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    Hospira, Inc.

    U.S.A
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    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75409

    Regulatory Info : DISCN

    Registration Country : USA

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    Hospira, Inc.

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    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML

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    Approval Date : 2000-06-20

    Application Number : 75409

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    IGI Labs, Inc.

    U.S.A
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    Brand Name : MIDAZOLAM HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2000-06-26

    Application Number : 75263

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    HLR

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    Brand Name : VERSED

    Dosage Form : INJECTABLE;INJECTION

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

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    Approval Date : 1985-12-20

    Application Number : 18654

    Regulatory Info : DISCN

    Registration Country : USA

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    HLR

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    Brand Name : VERSED

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1987-05-26

    Application Number : 18654

    Regulatory Info : DISCN

    Registration Country : USA

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.