01 2ALOSETRON HYDROCHLORIDE
02 2AMIFOSTINE
03 2ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE
04 1AURANOFIN
05 2AZATHIOPRINE
06 1CLOCORTOLONE PIVALATE
07 1CROTAMITON
08 1HYDROCORTISONE
09 2HYDROCORTISONE ACETATE
10 4HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
11 4NAFTIFINE HYDROCHLORIDE
12 1PAROXETINE MESYLATE
13 4PIRFENIDONE
14 11SOTALOL HYDROCHLORIDE
15 5TIZANIDINE HYDROCHLORIDE
01 38LEGACY PHARMA
02 5LEGACY PHARMA USA
01 6CAPSULE;ORAL
02 7CREAM;TOPICAL
03 2GEL;TOPICAL
04 2INJECTABLE;INJECTION
05 4LOTION;TOPICAL
06 22TABLET;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06 11% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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16 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 2267MG
18 1320MG
19 1375MG/VIAL
20 13MG
21 140MG
22 1500MG/VIAL
23 150MG
24 1534MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
25 160MG
26 1801MG
27 280MG
28 1EQ 0.5MG BASE
29 1EQ 1MG BASE
30 1EQ 2MG BASE
31 1EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
32 2EQ 4MG BASE
33 1EQ 6MG BASE
34 1EQ 7.5MG BASE
01 43USA
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 : RX
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : ETHYOL
Dosage Strength : 500MG/VIAL
Packaging :
Approval Date : 1995-12-08
Application Number : 20221
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : INJECTABLE;INJECTION
Brand Name : ETHYOL
Dosage Strength : 375MG/VIAL
Packaging :
Approval Date : 1999-09-10
Application Number : 20221
Regulatory Info : DISCN
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
