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01 1ACETIC ACID, GLACIAL; HYDROCORTISONE
02 2CHLORPROMAZINE HYDROCHLORIDE
03 1CLOBETASOL PROPIONATE
04 1CYCLOSPORINE
05 1HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
06 1METFORMIN HYDROCHLORIDE
07 1METRONIDAZOLE
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01 2CONCENTRATE;ORAL
02 1EMULSION;OPHTHALMIC
03 2SOLUTION/DROPS;OTIC
04 1SOLUTION;ORAL
05 1SOLUTION;TOPICAL
06 1SUSPENSION;ORAL
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01 20.05%
02 11%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
03 1100MG/ML
04 12%;1%
05 130MG/ML
06 2500MG/5ML
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01 3DISCN
02 5RX
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RLD : Yes
TE Code : AT
ACETIC ACID, GLACIAL; HYDROCORTISONE
Dosage Form : SOLUTION/DROPS; OTIC
Proprietary Name : VOSOL HC
Dosage Strength : 2%;1%
Approval Date : 1982-01-01
Application Number : 12770
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AT

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RLD : No
TE Code :
Dosage Form : CONCENTRATE; ORAL
Proprietary Name : SONAZINE
Dosage Strength : 30MG/ML
Approval Date : 1982-01-01
Application Number : 80983
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code :
Dosage Form : CONCENTRATE; ORAL
Proprietary Name : SONAZINE
Dosage Strength : 100MG/ML
Approval Date : 1982-01-01
Application Number : 80983
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code : AT
Dosage Form : SOLUTION; TOPICAL
Proprietary Name : CLOBETASOL PROPIONATE
Dosage Strength : 0.05%
Approval Date : 2019-10-02
Application Number : 211494
RX/OTC/DISCN : RX
RLD : No
TE Code : AT

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RLD : No
TE Code : AB
Dosage Form : EMULSION; OPHTHALMIC
Proprietary Name : CYCLOSPORINE
Dosage Strength : 0.05%
Approval Date : 2024-07-05
Application Number : 211943
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code :
HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Dosage Form : SOLUTION/DROPS; OTIC
Proprietary Name : NEOMYCIN AND POLYMYXIN B...
Dosage Strength : 1%;EQ 3.5MG BASE/ML;10,0...
Approval Date : 2005-10-31
Application Number : 65216
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code : AB
Dosage Form : SOLUTION; ORAL
Proprietary Name : METFORMIN HYDROCHLORIDE
Dosage Strength : 500MG/5ML
Approval Date : 2020-03-03
Application Number : 211309
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : Yes
TE Code :
Dosage Form : SUSPENSION; ORAL
Proprietary Name : LIKMEZ
Dosage Strength : 500MG/5ML
Approval Date : 2023-09-22
Application Number : 216755
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
