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01 3FRESENIUS KABI USA

02 3HIKMA

03 3MYLAN INSTITUTIONAL

04 3NIVAGEN PHARMS INC

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PharmaCompass

01

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REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/VIAL

Approval Date : 2018-01-16

Application Number : 206223

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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02

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Luxepack
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REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/VIAL

Approval Date : 2018-01-16

Application Number : 206223

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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03

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Luxepack
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REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 5MG BASE/VIAL

Approval Date : 2018-01-16

Application Number : 206223

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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04

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Luxepack
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REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/VIAL

Approval Date : 2020-10-13

Application Number : 210594

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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05

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Luxepack
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REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/VIAL

Approval Date : 2020-10-13

Application Number : 210594

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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06

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 5MG BASE/VIAL

Approval Date : 2020-10-13

Application Number : 210594

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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07

Luxepack
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Luxepack
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REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/VIAL

Approval Date : 2024-06-28

Application Number : 215635

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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08

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REMIFENTANIL HYDROCHLORIDE

Brand Name : ULTIVA

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/VIAL

Approval Date : 1996-07-12

Application Number : 20630

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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09

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : ULTIVA

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/VIAL

Approval Date : 1996-07-12

Application Number : 20630

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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10

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : ULTIVA

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 5MG BASE/VIAL

Approval Date : 1996-07-12

Application Number : 20630

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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