01 1CLOCORTOLONE PIVALATE
02 1CROTAMITON
03 1HYDROCORTISONE
04 11SOTALOL HYDROCHLORIDE
05 5TIZANIDINE HYDROCHLORIDE
01 14LEGACY PHARMA
02 5LEGACY PHARMA USA
01 3CAPSULE;ORAL
02 1CREAM;TOPICAL
03 2LOTION;TOPICAL
04 13TABLET;ORAL
01 10.1%
02 110%
03 1100MG
04 2120MG
05 2160MG
06 12%
07 1240MG
08 1320MG
09 140MG
10 160MG
11 280MG
12 1EQ 2MG BASE
13 1EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
14 2EQ 4MG BASE
15 1EQ 6MG BASE
01 19USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CREAM;TOPICAL
Brand Name : CLODERM
Dosage Strength : 0.1%
Packaging :
Approval Date : 1982-01-01
Application Number : 17765
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : LOTION;TOPICAL
Brand Name : CROTAN
Dosage Strength : 10%
Packaging :
Approval Date : 1982-01-01
Application Number : 87204
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : LOTION;TOPICAL
Brand Name : ALA-SCALP
Dosage Strength : 2%
Packaging :
Approval Date : 1982-01-01
Application Number : 83231
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BETAPACE
Dosage Strength : 80MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19865
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BETAPACE
Dosage Strength : 160MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19865
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BETAPACE
Dosage Strength : 320MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19865
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BETAPACE AF
Dosage Strength : 120MG
Packaging :
Approval Date : 2000-02-22
Application Number : 21151
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BETAPACE AF
Dosage Strength : 100MG
Packaging :
Approval Date : 2003-03-14
Application Number : 21151
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BETAPACE AF
Dosage Strength : 40MG
Packaging :
Approval Date : 2003-04-02
Application Number : 21151
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BETAPACE AF
Dosage Strength : 60MG
Packaging :
Approval Date : 2003-04-02
Application Number : 21151
Regulatory Info : DISCN
Registration Country : USA
LOOKING FOR A SUPPLIER?