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01 2BUPROPION HYDROCHLORIDE
02 1CYPROHEPTADINE HYDROCHLORIDE
03 3DIVALPROEX SODIUM
04 1FLUOCINOLONE ACETONIDE
05 1METHYLPREDNISOLONE
06 3PROMETHAZINE HYDROCHLORIDE
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01 1CREAM;TOPICAL
02 1SYRUP;ORAL
03 3TABLET, DELAYED RELEASE;ORAL
04 6TABLET;ORAL
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01 10.025%
02 1100MG
03 112.5MG
04 125MG
05 12MG/5ML
06 14MG
07 150MG
08 175MG
09 1EQ 125MG VALPROIC ACID
10 1EQ 250MG VALPROIC ACID
11 1EQ 500MG VALPROIC ACID
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01 7DISCN
02 4RX
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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 100MG
Approval Date : 2000-10-10
Application Number : 75613
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 75MG
Approval Date : 2000-10-10
Application Number : 75613
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code : AA
Dosage Form : SYRUP; ORAL
Proprietary Name : CYPROHEPTADINE HYDROCHLO...
Dosage Strength : 2MG/5ML
Approval Date : 2018-10-16
Application Number : 209108
RX/OTC/DISCN : RX
RLD : No
TE Code : AA

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RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 500MG VALPROIC ACID
Approval Date : 2008-07-29
Application Number : 78290
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 250MG VALPROIC ACID
Approval Date : 2008-07-29
Application Number : 78290
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 125MG VALPROIC ACID
Approval Date : 2008-07-29
Application Number : 78290
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code :
Dosage Form : CREAM; TOPICAL
Proprietary Name : FLUOCINOLONE ACETONIDE
Dosage Strength : 0.025%
Approval Date : 1982-12-16
Application Number : 88045
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : METHYLPREDNISOLONE
Dosage Strength : 4MG
Approval Date : 1982-01-01
Application Number : 87341
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : PROMETHAZINE HYDROCHLORI...
Dosage Strength : 25MG
Approval Date : 1982-01-01
Application Number : 85146
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : PROMETHAZINE HYDROCHLORI...
Dosage Strength : 50MG
Approval Date : 1982-01-01
Application Number : 85146
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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