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01 1DOCOSANOL
02 3IBUPROFEN
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01 1AVEMA PHARMA
02 2P AND L DEV LLC
03 1P AND L DEVELOPMENT
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01 1CAPSULE;ORAL
02 1CREAM;TOPICAL
03 2TABLET;ORAL
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01 110%
02 2200MG
03 1EQ 200MG FREE ACID AND POTASSIUM SALT
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01 4USA
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Regulatory Info : OTC
Registration Country : USA
P and L Development of New York Corporation
Dosage Form : CREAM;TOPICAL
Brand Name : DOCOSANOL
Dosage Strength : 10%
Packaging :
Approval Date : 2022-10-07
Application Number : 212385
Regulatory Info : OTC
Registration Country : USA

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Regulatory Info : DISCN
Registration Country : USA
P and L Development of New York Corporation
Dosage Form : TABLET;ORAL
Brand Name : IBUPROFEN
Dosage Strength : 200MG
Packaging :
Approval Date : 1986-09-19
Application Number : 70733
Regulatory Info : DISCN
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : OTC
Registration Country : USA
P and L Development of New York Corporation
Dosage Form : TABLET;ORAL
Brand Name : IBUPROFEN
Dosage Strength : 200MG
Packaging :
Approval Date : 2003-11-26
Application Number : 76460
Regulatory Info : OTC
Registration Country : USA

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : OTC
Registration Country : USA
P and L Development of New York Corporation
Dosage Form : CAPSULE;ORAL
Brand Name : IBUPROFEN
Dosage Strength : EQ 200MG FREE ACID AND...
Packaging :
Approval Date : 2009-07-10
Application Number : 77338
Regulatory Info : OTC
Registration Country : USA
