01 1ALBUTEROL SULFATE
02 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE
03 1BROMFENAC SODIUM
04 1CIPROFLOXACIN; DEXAMETHASONE
05 1ERYTHROMYCIN
06 1KETOTIFEN FUMARATE
07 1LIDOCAINE HYDROCHLORIDE
08 3LOTEPREDNOL ETABONATE
09 1OFLOXACIN
10 1TIMOLOL MALEATE
01 1GEL;OPHTHALMIC
02 1JELLY;TOPICAL
03 1OINTMENT;OPHTHALMIC
04 5SOLUTION/DROPS;OPHTHALMIC
05 1SOLUTION;INHALATION
06 2SUSPENSION/DROPS;OPHTHALMIC
07 1SUSPENSION/DROPS;OTIC
01 10.2%
02 10.2%;EQ 0.5% BASE
03 10.3%
04 10.3%;0.1%
05 30.5%
06 12%
07 1EQ 0.025% BASE
08 1EQ 0.09% ACID
09 2EQ 0.5% BASE
01 1OTC
02 11RX
RLD : No
TE Code : AN
Dosage Form : SOLUTION; INHALATION
Proprietary Name : ALBUTEROL SULFATE
Dosage Strength : EQ 0.5% BASE
Approval Date : 1998-01-15
Application Number : 74543
RX/OTC/DISCN : RX
RLD : No
TE Code : AN
RLD : No
TE Code : AB
BRIMONIDINE TARTRATE; TIMOLOL MALEATE
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : BRIMONIDINE TARTRATE AND...
Dosage Strength : 0.2%;EQ 0.5% BASE
Approval Date : 2022-10-31
Application Number : 91086
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AT2
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : BROMFENAC SODIUM
Dosage Strength : EQ 0.09% ACID
Approval Date : 2014-01-22
Application Number : 203395
RX/OTC/DISCN : RX
RLD : No
TE Code : AT2
RLD : No
TE Code : AB
Dosage Form : SUSPENSION/DROPS; OTIC
Proprietary Name : CIPROFLOXACIN AND DEXAME...
Dosage Strength : 0.3%;0.1%
Approval Date : 2023-06-09
Application Number : 215768
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AT
Dosage Form : OINTMENT; OPHTHALMIC
Proprietary Name : ERYTHROMYCIN
Dosage Strength : 0.5%
Approval Date : 1996-07-18
Application Number : 64030
RX/OTC/DISCN : RX
RLD : No
TE Code : AT
RLD : No
TE Code :
Dosage Form : SOLUTION/DROPS; OPHTHALMIC
Proprietary Name : KETOTIFEN FUMARATE
Dosage Strength : EQ 0.025% BASE
Approval Date : 2007-07-26
Application Number : 77958
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : No
TE Code : AT
Dosage Form : JELLY; TOPICAL
Proprietary Name : LIDOCAINE HYDROCHLORIDE
Dosage Strength : 2%
Approval Date : 2003-02-12
Application Number : 40433
RX/OTC/DISCN : RX
RLD : No
TE Code : AT
RLD : No
TE Code : AB
Dosage Form : SUSPENSION/DROPS; OPHTHALMIC
Proprietary Name : LOTEPREDNOL ETABONATE
Dosage Strength : 0.5%
Approval Date : 2019-04-17
Application Number : 207609
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : GEL; OPHTHALMIC
Proprietary Name : LOTEPREDNOL ETABONATE
Dosage Strength : 0.5%
Approval Date : 2021-02-10
Application Number : 212080
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : SUSPENSION/DROPS; OPHTHALMIC
Proprietary Name : LOTEPREDNOL ETABONATE
Dosage Strength : 0.2%
Approval Date : 2023-04-12
Application Number : 215933
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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