01 2ECR Pharmaceuticals Co Inc
02 1Neos Therapeutics
03 1Tris Pharma Inc
04 1UCB Pharma S.A
01 2CAPSULE, EXTENDED RELEASE;ORAL
02 3SUSPENSION, EXTENDED RELEASE;ORAL
01 4DISCN
02 1RX
01 1HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX
02 1HYDROCODONE POLISTIREX AND CHLORPHENIRAMNE POLISTIREX
03 2TUSSICAPS
04 1TUSSIONEX PENNKINETIC
01 5USA
Regulatory Info : DISCN
Registration Country : USA
CHLORPHENIRAMINE POLISTIREX; HYDROCODONE POLISTIREX
Brand Name : TUSSICAPS
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 8MG MALEATE;EQ 10MG BITARTRATE
Packaging :
Approval Date : 2007-09-24
Application Number : 77273
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CHLORPHENIRAMINE POLISTIREX; HYDROCODONE POLISTIREX
Brand Name : TUSSICAPS
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 4MG MALEATE;EQ 5MG BITARTRATE
Packaging :
Approval Date : 2007-09-24
Application Number : 77273
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CHLORPHENIRAMINE POLISTIREX; HYDROCODONE POLISTIREX
Brand Name : HYDROCODONE POLISTIREX AND CHLORPHENIRAMNE POLISTIREX
Dosage Form : SUSPENSION, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 8MG MALEATE/5ML;EQ 10MG BITARTRATE/5ML
Packaging :
Approval Date : 2012-06-29
Application Number : 91671
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
CHLORPHENIRAMINE POLISTIREX; HYDROCODONE POLISTIREX
Brand Name : HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX
Dosage Form : SUSPENSION, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 8MG MALEATE/5ML;EQ 10MG BITARTRATE/5ML
Packaging :
Approval Date : 2010-10-01
Application Number : 91632
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CHLORPHENIRAMINE POLISTIREX; HYDROCODONE POLISTIREX
Brand Name : TUSSIONEX PENNKINETIC
Dosage Form : SUSPENSION, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 8MG MALEATE/5ML;EQ 10MG BITARTRATE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1987-12-31
Application Number : 19111
Regulatory Info : DISCN
Registration Country : USA
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