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01 1CLINDAMYCIN PHOSPHATE
02 3ERYTHROMYCIN ETHYLSUCCINATE
03 2ETRAVIRINE
04 1LETROZOLE
05 3LOMUSTINE
06 2RASAGILINE MESYLATE
07 1VIGABATRIN
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01 3CAPSULE;ORAL
02 3GRANULE;ORAL
03 1SWAB;TOPICAL
04 6TABLET;ORAL
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01 2100MG
02 110MG
03 12.5MG
04 1200MG
05 140MG
06 1500MG
07 1EQ 0.5MG BASE
08 1EQ 1% BASE
09 1EQ 1MG BASE
10 2EQ 200MG BASE/5ML
11 1EQ 400MG BASE/5ML
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01 1DISCN
02 12RX
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RLD : No
TE Code : AT
Dosage Form : SWAB; TOPICAL
Proprietary Name : CLINDAMYCIN PHOSPHATE
Dosage Strength : EQ 1% BASE
Approval Date : 2025-06-13
Application Number : 219612
RX/OTC/DISCN : RX
RLD : No
TE Code : AT

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RLD : Yes
TE Code : AB
Dosage Form : GRANULE; ORAL
Proprietary Name : E.E.S.
Dosage Strength : EQ 200MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 50207
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

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RLD : Yes
TE Code : AB
Dosage Form : GRANULE; ORAL
Proprietary Name : ERYPED
Dosage Strength : EQ 400MG BASE/5ML
Approval Date : 1982-01-01
Application Number : 50207
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

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RLD : Yes
TE Code : AB
Dosage Form : GRANULE; ORAL
Proprietary Name : ERYPED
Dosage Strength : EQ 200MG BASE/5ML
Approval Date : 1987-03-30
Application Number : 50207
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ETRAVIRINE
Dosage Strength : 100MG
Approval Date : 2022-04-13
Application Number : 215402
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : ETRAVIRINE
Dosage Strength : 200MG
Approval Date : 2022-04-13
Application Number : 215402
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : LETROZOLE
Dosage Strength : 2.5MG
Approval Date : 2011-06-03
Application Number : 91191
RX/OTC/DISCN : DISCN
RLD : No
TE Code :

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LOMUSTINE
Dosage Strength : 10MG
Approval Date : 2025-10-27
Application Number : 219265
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LOMUSTINE
Dosage Strength : 40MG
Approval Date : 2025-10-27
Application Number : 219265
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : LOMUSTINE
Dosage Strength : 100MG
Approval Date : 2025-10-27
Application Number : 219265
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
