01 1FOUGERA PHARMS
02 1GLAXOSMITHKLINE
03 1GLENMARK PHARMS
04 1PADAGIS ISRAEL
05 1PADAGIS US
06 1TARO
07 1TEVA
01 7OINTMENT;TOPICAL
01 1DISCN
02 6RX
01 1BACTROBAN
02 1CENTANY
03 5MUPIROCIN
01 6No
02 1Yes
RLD : No
TE Code : AB
Brand Name : MUPIROCIN
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 2%
Approval Date : 2005-11-30
Application Number : 65192
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : MUPIROCIN
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 2%
Approval Date : 2011-06-08
Application Number : 90480
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : BACTROBAN
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1987-12-31
Application Number : 50591
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code : BX
Brand Name : CENTANY
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 2%
Approval Date : 2002-12-04
Application Number : 50788
RX/OTC/DISCN : RX
RLD : No
TE Code : BX
RLD : No
TE Code : AB
Brand Name : MUPIROCIN
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 2%
Approval Date : 2003-11-07
Application Number : 65123
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : MUPIROCIN
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 2%
Approval Date : 2005-09-23
Application Number : 65170
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : MUPIROCIN
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 2%
Approval Date : 2003-11-07
Application Number : 65085
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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