01 1CLOCORTOLONE PIVALATE
02 1CROTAMITON
03 1HYDROCORTISONE
04 11SOTALOL HYDROCHLORIDE
05 5TIZANIDINE HYDROCHLORIDE
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13 1EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 5DISCN
02 14RX
RLD : Yes
TE Code : AB
Dosage Form : CREAM; TOPICAL
Proprietary Name : CLODERM
Dosage Strength : 0.1%
Approval Date : 1982-01-01
Application Number : 17765
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code : AT
Dosage Form : LOTION; TOPICAL
Proprietary Name : CROTAN
Dosage Strength : 10%
Approval Date : 1982-01-01
Application Number : 87204
RX/OTC/DISCN : RX
RLD : No
TE Code : AT
RLD : No
TE Code :
Dosage Form : LOTION; TOPICAL
Proprietary Name : ALA-SCALP
Dosage Strength : 2%
Approval Date : 1982-01-01
Application Number : 83231
RX/OTC/DISCN : RX
RLD : No
TE Code :
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BETAPACE
Dosage Strength : 80MG
Approval Date : 1992-10-30
Application Number : 19865
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BETAPACE
Dosage Strength : 160MG
Approval Date : 1992-10-30
Application Number : 19865
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BETAPACE AF
Dosage Strength : 80MG
Approval Date : 2000-02-22
Application Number : 21151
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BETAPACE AF
Dosage Strength : 120MG
Approval Date : 2000-02-22
Application Number : 21151
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : BETAPACE AF
Dosage Strength : 160MG
Approval Date : 2000-02-22
Application Number : 21151
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BETAPACE AF
Dosage Strength : 100MG
Approval Date : 2003-03-14
Application Number : 21151
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BETAPACE AF
Dosage Strength : 40MG
Approval Date : 2003-04-02
Application Number : 21151
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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