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01 3ASTRAL

02 3B BRAUN MEDICAL

03 3BAXTER HLTHCARE CORP

04 2EUGIA PHARMA

05 3EUGIA PHARMA SPECLTS

06 4FRESENIUS KABI

07 1FRESENIUS KABI USA

08 4HOSPIRA INC

09 8ISTITUTO BIO ITA SPA

10 3ONESOURCE SPECIALTY

11 5PROVEPHARM SAS

12 4SAGENT PHARMS INC

13 8SANDOZ

14 4SHANDONG

15 4WOCKHARDT BIO AG

16 4WYETH PHARMS

17 7WYETH PHARMS INC

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PharmaCompass

01

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Brand Name : ZOSYN IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40MG BASE/ML;EQ 5MG BASE/ML

Approval Date : 1998-02-24

Application Number : 50750

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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02

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Brand Name : ZOSYN IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 60MG BASE/ML;EQ 7.5MG BASE/ML

Approval Date : 1998-02-24

Application Number : 50750

RX/OTC/DISCN : RX

RLD : Yes

TE Code :

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03

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM

Brand Name : PIPRACIL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 50545

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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04

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM

Brand Name : PIPRACIL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 3GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 50545

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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05

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM

Brand Name : PIPRACIL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 50545

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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06

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM

Brand Name : PIPRACIL

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 40GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1985-09-30

Application Number : 50545

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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07

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Brand Name : ZOSYN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2GM BASE/VIAL;EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1993-10-22

Application Number : 50684

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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08

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Brand Name : ZOSYN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 3GM BASE/VIAL;EQ 375MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1993-10-22

Application Number : 50684

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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09

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Brand Name : ZOSYN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 4GM BASE/VIAL;EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1993-10-22

Application Number : 50684

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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10

Discovery Europe
Not Confirmed
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Discovery Europe
Not Confirmed

PIPERACILLIN SODIUM; TAZOBACTAM SODIUM

Brand Name : ZOSYN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1993-10-22

Application Number : 50684

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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