01 2BUPROPION HYDROCHLORIDE
02 3DIVALPROEX SODIUM
03 1FLUOCINOLONE ACETONIDE
04 2GABAPENTIN
05 1MECLIZINE HYDROCHLORIDE
06 1METHYLPREDNISOLONE
07 3PROMETHAZINE HYDROCHLORIDE
01 13INVATECH
01 1CREAM;TOPICAL
02 3TABLET, DELAYED RELEASE;ORAL
03 9TABLET;ORAL
01 10.025%
02 1100MG
03 112.5MG
04 225MG
05 14MG
06 150MG
07 1600MG
08 175MG
09 1800MG
10 1EQ 125MG VALPROIC ACID
11 1EQ 250MG VALPROIC ACID
12 1EQ 500MG VALPROIC ACID
01 13USA
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 : GABAPENTIN
Dosage Strength : 600MG
Packaging :
Approval Date : 2006-07-06
Application Number : 76877
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : GABAPENTIN
Dosage Strength : 800MG
Packaging :
Approval Date : 2006-07-06
Application Number : 76877
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : MECLIZINE HYDROCHLORIDE
Dosage Strength : 25MG
Packaging :
Approval Date : 1989-05-22
Application Number : 84092
Regulatory Info : RX
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
LOOKING FOR A SUPPLIER?