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01 2BUPROPION HYDROCHLORIDE
02 3DIVALPROEX SODIUM
03 1FLUOCINOLONE ACETONIDE
04 1METHYLPREDNISOLONE
05 3PROMETHAZINE HYDROCHLORIDE
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01 10INVATECH
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01 1CREAM;TOPICAL
02 3TABLET, DELAYED RELEASE;ORAL
03 6TABLET;ORAL
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01 10.025%
02 1100MG
03 112.5MG
04 125MG
05 14MG
06 150MG
07 175MG
08 1EQ 125MG VALPROIC ACID
09 1EQ 250MG VALPROIC ACID
10 1EQ 500MG VALPROIC ACID
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01 10USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 100MG
Packaging :
Approval Date : 2000-10-10
Application Number : 75613
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUPROPION HYDROCHLORIDE
Dosage Strength : 75MG
Packaging :
Approval Date : 2000-10-10
Application Number : 75613
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, DELAYED RELEASE;...
Brand Name : DIVALPROEX SODIUM
Dosage Strength : EQ 500MG VALPROIC ACID
Packaging :
Approval Date : 2008-07-29
Application Number : 78290
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, DELAYED RELEASE;...
Brand Name : DIVALPROEX SODIUM
Dosage Strength : EQ 250MG VALPROIC ACID
Packaging :
Approval Date : 2008-07-29
Application Number : 78290
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET, DELAYED RELEASE;...
Brand Name : DIVALPROEX SODIUM
Dosage Strength : EQ 125MG VALPROIC ACID
Packaging :
Approval Date : 2008-07-29
Application Number : 78290
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : FLUOCINOLONE ACETONIDE
Dosage Strength : 0.025%
Packaging :
Approval Date : 1982-12-16
Application Number : 88045
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : METHYLPREDNISOLONE
Dosage Strength : 4MG
Packaging :
Approval Date : 1982-01-01
Application Number : 87341
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PROMETHAZINE HYDROCHLORID...
Dosage Strength : 12.5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 84233
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PROMETHAZINE HYDROCHLORID...
Dosage Strength : 25MG
Packaging :
Approval Date : 1982-01-01
Application Number : 85146
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : PROMETHAZINE HYDROCHLORID...
Dosage Strength : 50MG
Packaging :
Approval Date : 1982-01-01
Application Number : 85146
Regulatory Info : DISCN
Registration Country : USA