01 2ALOSETRON HYDROCHLORIDE
02 2ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
03 1AURANOFIN
04 2AZATHIOPRINE
05 1CLOCORTOLONE PIVALATE
06 1CROTAMITON
07 1HYDROCORTISONE
08 2HYDROCORTISONE ACETATE
09 4HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
10 4NAFTIFINE HYDROCHLORIDE
11 1PAROXETINE MESYLATE
12 11SOTALOL HYDROCHLORIDE
13 5TIZANIDINE HYDROCHLORIDE
01 32LEGACY PHARMA
02 5LEGACY PHARMA USA
01 5CAPSULE;ORAL
02 7CREAM;TOPICAL
03 2GEL;TOPICAL
04 4LOTION;TOPICAL
05 19TABLET;ORAL
01 10.025MG;0.5MG
02 10.025MG;1MG
03 10.1%
04 10.5%;1%
05 11%
06 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 21%;1%
08 110%
09 1100MG
10 2120MG
11 2160MG
12 42%
13 12.5%
14 12.5%;1%
15 1240MG
16 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
17 1320MG
18 13MG
19 140MG
20 150MG
21 160MG
22 280MG
23 1EQ 0.5MG BASE
24 1EQ 1MG BASE
25 1EQ 2MG BASE
26 1EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 2EQ 4MG BASE
28 1EQ 6MG BASE
29 1EQ 7.5MG BASE
01 37USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : LOTRONEX
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date : 2000-02-09
Application Number : 21107
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : LOTRONEX
Dosage Strength : EQ 0.5MG BASE
Packaging :
Approval Date : 2003-12-23
Application Number : 21107
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : MOTOFEN HALF-STRENGTH
Dosage Strength : 0.025MG;0.5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 17744
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : MOTOFEN
Dosage Strength : 0.025MG;1MG
Packaging :
Approval Date : 1982-01-01
Application Number : 17744
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : CAPSULE;ORAL
Brand Name : RIDAURA
Dosage Strength : 3MG
Packaging :
Approval Date : 1985-05-24
Application Number : 18689
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : IMURAN
Dosage Strength : 50MG
Packaging :
Approval Date : 1982-01-01
Application Number : 16324
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : IMURAN
Dosage Strength : 25MG **Federal Registe...
Packaging :
Approval Date : 1982-01-01
Application Number : 16324
Regulatory Info : DISCN
Registration Country : USA
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
