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01 1Alembic Pharmaceuticals Limited

02 1Amneal Pharmaceuticals

03 1Encube Ethicals

04 3GSK

05 3Glenmark Pharmaceuticals

06 1Kolmar Korea Co., Ltd.

07 1Padagis

08 1Parallel Pharma Ab

09 1Taro Pharmaceutical Industries

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PharmaCompass

01

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
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MUPIROCIN CALCIUM

Brand Name : MUPIROCIN

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 2% BASE

Packaging :

Approval Date : 2021-11-16

Application Number : 213053

Regulatory Info : RX

Registration Country : USA

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02

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

MUPIROCIN CALCIUM

Brand Name : MUPIROCIN

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 2% BASE

Packaging :

Approval Date : 2022-11-15

Application Number : 214811

Regulatory Info : RX

Registration Country : USA

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03

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

MUPIROCIN CALCIUM

Brand Name : MUPIROCIN

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 2% BASE

Packaging :

Approval Date : 2021-08-31

Application Number : 213076

Regulatory Info : RX

Registration Country : USA

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04

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

MUPIROCIN CALCIUM

Brand Name : MUPIROCIN

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 2% BASE

Packaging :

Approval Date : 2013-01-24

Application Number : 201587

Regulatory Info : RX

Registration Country : USA

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05

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

Mupirocin calcium

Brand Name : Supiroban Cream

Dosage Form : CRE

Dosage Strength : 20mg/g

Packaging : 15X1mg/g

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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06

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

Mupirocin calcium

Brand Name : Supiroban Cream

Dosage Form : CRE

Dosage Strength : 20mg/g

Packaging : 30X1mg/g

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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07

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

MUPIROCIN CALCIUM

Brand Name : BACTROBAN

Dosage Form : OINTMENT;NASAL

Dosage Strength : EQ 2% BASE

Packaging :

Approval Date : 1995-09-18

Application Number : 50703

Regulatory Info : DISCN

Registration Country : USA

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08

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

MUPIROCIN CALCIUM

Brand Name : BACTROBAN

Dosage Form : CREAM;TOPICAL

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

Packaging :

Approval Date : 1997-12-11

Application Number : 50746

Regulatory Info : DISCN

Registration Country : USA

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09

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

Mupirocin Calcium

Brand Name : Bactroban Nasal

Dosage Form : Salve

Dosage Strength : 0.02

Packaging :

Approval Date : 29/04/1993

Application Number : 19930429000108

Regulatory Info : Approved

Registration Country : Sweden

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10

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

Mupirocin Calcium

Brand Name : Mupirocin Nasal Ointment

Dosage Form : Nasal Ointment

Dosage Strength : 21.5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : South Korea

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11

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

MUPIROCIN CALCIUM

Brand Name : MUPIROCIN

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 2% BASE

Packaging :

Approval Date : 2022-08-03

Application Number : 212465

Regulatory Info : DISCN

Registration Country : USA

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12

AIChE Annual Meeting
Not Confirmed
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AIChE Annual Meeting
Not Confirmed

MUPIROCIN CALCIUM

Brand Name : MUPIROCIN

Dosage Form : CREAM;TOPICAL

Dosage Strength : EQ 2% BASE

Packaging :

Approval Date : 2020-04-27

Application Number : 207116

Regulatory Info : RX

Registration Country : USA

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13

Parallel Pharma Ab

Country
AIChE Annual Meeting
Not Confirmed
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Parallel Pharma Ab

Country
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AIChE Annual Meeting
Not Confirmed

Mupirocin Calcium

Brand Name : Bactroban Nasal

Dosage Form : Salve

Dosage Strength :

Packaging :

Approval Date : 16/11/2007

Application Number : 20070213000016

Regulatory Info : Deregistered

Registration Country : Sweden

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