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Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMIODARONE HYDROCHLORIDE
Dosage Strength : 50MG/ML
Packaging :
Approval Date : 2008-10-30
Application Number : 77610
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : AMIODARONE HYDROCHLORIDE
Dosage Strength : 50MG/ML
Packaging :
Approval Date : 2008-10-30
Application Number : 77834
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : BENZONATATE
Dosage Strength : 200MG
Packaging :
Approval Date : 2015-01-16
Application Number : 91310
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : BENZONATATE
Dosage Strength : 100MG
Packaging :
Approval Date : 2015-01-16
Application Number : 91310
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION/DROPS;OPHTHALMI...
Brand Name : BETAXOLOL HYDROCHLORIDE
Dosage Strength : EQ 0.5% BASE
Packaging :
Approval Date : 2009-11-16
Application Number : 78694
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : SYRUP;ORAL
Brand Name : BROMPHENIRAMINE MALEATE, ...
Dosage Strength : 2MG/5ML;10MG/5ML;30MG/...
Packaging :
Approval Date : 2016-09-20
Application Number : 203375
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CHLORPHENIRAMINE MALEATE; HYDROCODONE BITARTRATE
Dosage Form : SOLUTION;ORAL
Brand Name : HYDROCODONE BITARTRATE AN...
Dosage Strength : 4MG/5ML;5MG/5ML
Packaging :
Approval Date : 2017-06-09
Application Number : 206891
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;TOPICAL
Brand Name : CICLOPIROX
Dosage Strength : 8%
Packaging :
Approval Date : 2007-09-18
Application Number : 78172
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : DOXYCYCLINE HYCLATE
Dosage Strength : EQ 100MG BASE
Packaging :
Approval Date : 2020-03-16
Application Number : 210664
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : DUTASTERIDE
Dosage Strength : 0.5MG
Packaging :
Approval Date : 2016-03-17
Application Number : 206373
Regulatory Info : RX
Registration Country : USA
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