01 1DOCOSANOL
02 3IBUPROFEN
01 1AVEMA PHARMA
02 2P AND L DEV LLC
03 1P AND L DEVELOPMENT
01 1CAPSULE;ORAL
02 1CREAM;TOPICAL
03 2TABLET;ORAL
01 110%
02 2200MG
03 1EQ 200MG FREE ACID AND POTASSIUM SALT
01 4USA
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
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
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
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
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