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01 2ACS DOBFAR

02 3HOSPIRA INC

03 1HQ SPCLT PHARMA

04 6MERCK

05 1MSD MERCK CO

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PharmaCompass

01

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : IMIPENEM AND CILASTATIN

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL

Approval Date : 2011-12-21

Application Number : 90577

RX/OTC/DISCN : RX

RLD : No

TE Code :

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02

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : IMIPENEM AND CILASTATIN

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

Approval Date : 2011-12-21

Application Number : 90577

RX/OTC/DISCN : RX

RLD : No

TE Code : AP

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03

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : IMIPENEM AND CILASTATIN

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL

Approval Date : 2011-11-16

Application Number : 90825

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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04

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : IMIPENEM AND CILASTATIN

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

Approval Date : 2011-11-16

Application Number : 90825

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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05

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : PRIMAXIN

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1985-11-26

Application Number : 50587

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : PRIMAXIN

Dosage Form : POWDER;INTRAVENOUS

Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

Approval Date : 1985-11-26

Application Number : 50587

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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07

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : PRIMAXIN

Dosage Form : POWDER;INTRAMUSCULAR

Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

Approval Date : 1990-12-14

Application Number : 50630

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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08

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : PRIMAXIN

Dosage Form : POWDER;INTRAMUSCULAR

Dosage Strength : EQ 750MG BASE/VIAL;750MG/VIAL

Approval Date : 1990-12-14

Application Number : 50630

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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09

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : PRIMAXIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 250MG BASE/VIAL;250MG/VIAL

Approval Date : 1987-01-08

Application Number : 62756

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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10

Pharmtech & Ingredients
Not Confirmed
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Pharmtech & Ingredients
Not Confirmed

CILASTATIN SODIUM; IMIPENEM

Brand Name : PRIMAXIN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 500MG BASE/VIAL;500MG/VIAL

Approval Date : 1987-01-08

Application Number : 62756

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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