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01 1ACETAMINOPHEN; IBUPROFEN
02 2DIPHENHYDRAMINE HYDROCHLORIDE
03 1DOXYLAMINE SUCCINATE
04 3IBUPROFEN
05 1LOPERAMIDE HYDROCHLORIDE
06 1METRONIDAZOLE
07 1NAPROXEN SODIUM
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01 2CAPSULE;ORAL
02 8TABLET;ORAL
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01 1100MG
02 2200MG
03 1220MG
04 1250MG
05 1250MG;125MG
06 225MG
07 12MG
08 150MG
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01 4DISCN
02 5OTC
03 1Blank
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RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND IBUPRO...
Dosage Strength : 250MG;125MG
Approval Date :
Application Number : 220126
RX/OTC/DISCN :
RLD :
TE Code :

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RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : DIPHENHYDRAMINE HYDROCHL...
Dosage Strength : 25MG
Approval Date : 1983-01-27
Application Number : 87977
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : DIPHENHYDRAMINE HYDROCHL...
Dosage Strength : 50MG
Approval Date : 1983-01-27
Application Number : 87978
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DOXYLAMINE SUCCINATE
Dosage Strength : 25MG
Approval Date : 2004-08-27
Application Number : 40564
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 200MG
Approval Date : 1999-03-01
Application Number : 75010
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 200MG
Approval Date : 1999-03-01
Application Number : 75139
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 100MG
Approval Date : 2004-06-17
Application Number : 76741
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : LOPERAMIDE HYDROCHLORIDE
Dosage Strength : 2MG
Approval Date : 2003-06-10
Application Number : 76497
RX/OTC/DISCN : OTC
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : METRONIDAZOLE
Dosage Strength : 250MG
Approval Date : 1984-04-10
Application Number : 19029
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : NAPROXEN SODIUM
Dosage Strength : 220MG
Approval Date : 2017-01-23
Application Number : 204872
RX/OTC/DISCN : OTC
RLD : No
TE Code :

LNK is a supplier offers 1 products (APIs, Excipients or Intermediates).
Find a price of Ibuprofen bulk offered by LNK