01 1KETOROLAC TROMETHAMINE
02 6NAPROXEN
03 2NAPROXEN SODIUM
01 1SUSPENSION;ORAL
02 2TABLET, DELAYED RELEASE;ORAL
03 6TABLET;ORAL
01 110MG
02 1250MG
03 125MG/ML
04 2375MG
05 2500MG
06 1EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 1EQ 500MG BASE
01 3DISCN
02 6RX
RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : KETOROLAC TROMETHAMINE
Dosage Strength : 10MG
Approval Date : 2022-10-21
Application Number : 216407
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NAPROSYN
Dosage Strength : 250MG
Approval Date : 1982-01-01
Application Number : 17581
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NAPROSYN
Dosage Strength : 375MG
Approval Date : 1982-01-01
Application Number : 17581
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : NAPROSYN
Dosage Strength : 500MG
Approval Date : 1982-04-15
Application Number : 17581
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : SUSPENSION; ORAL
Proprietary Name : NAPROSYN
Dosage Strength : 25MG/ML
Approval Date : 1987-03-23
Application Number : 18965
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : EC-NAPROSYN
Dosage Strength : 375MG
Approval Date : 1994-10-14
Application Number : 20067
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : EC-NAPROSYN
Dosage Strength : 500MG
Approval Date : 1994-10-14
Application Number : 20067
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ANAPROX
Dosage Strength : EQ 250MG BASE **Federal ...
Approval Date : 1982-01-01
Application Number : 18164
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ANAPROX DS
Dosage Strength : EQ 500MG BASE
Approval Date : 1987-09-30
Application Number : 18164
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
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