01 1DOCOSANOL
02 3IBUPROFEN
01 1CAPSULE;ORAL
02 1CREAM;TOPICAL
03 2TABLET;ORAL
01 110%
02 2200MG
03 1EQ 200MG FREE ACID AND POTASSIUM SALT
01 1DISCN
02 3OTC
RLD : No
TE Code :
P and L Development of New York Corporation
Dosage Form : CREAM; TOPICAL
Proprietary Name : DOCOSANOL
Dosage Strength : 10%
Approval Date : 2022-10-07
Application Number : 212385
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
P and L Development of New York Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 200MG
Approval Date : 1986-09-19
Application Number : 70733
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
P and L Development of New York Corporation
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 200MG
Approval Date : 2003-11-26
Application Number : 76460
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code :
P and L Development of New York Corporation
Dosage Form : CAPSULE; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : EQ 200MG FREE ACID AND P...
Approval Date : 2009-07-10
Application Number : 77338
RX/OTC/DISCN : OTC
RLD : No
TE Code :
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