01 3ACCORD HLTHCARE
02 3ACTAVIS ELIZABETH
03 5ALEMBIC
04 3AUROBINDO PHARMA USA
05 5BARR
06 3CHARTWELL RX
07 5CHEPLAPHARM
08 5PH HEALTH
09 3PHARMOBEDIENT
10 3PRINSTON INC
11 5ROCHE
12 3RUBICON RESEARCH
13 3SANDOZ
14 8SUN PHARM INDS INC
15 6TEVA
16 3WATSON LABS
01 25TABLET, ORALLY DISINTEGRATING;ORAL
02 41TABLET;ORAL
01 24DISCN
02 42RX
01 56CLONAZEPAM
02 5KLONOPIN
03 5KLONOPIN RAPIDLY DISINTEGRATING
01 58No
02 8Yes
RLD : Yes
TE Code : AB
Brand Name : KLONOPIN
Dosage Form : TABLET;ORAL
Dosage Strength : 0.5MG
Approval Date : 1982-01-01
Application Number : 17533
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : KLONOPIN
Dosage Form : TABLET;ORAL
Dosage Strength : 1MG
Approval Date : 1982-01-01
Application Number : 17533
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : KLONOPIN
Dosage Form : TABLET;ORAL
Dosage Strength : 2MG
Approval Date : 1982-01-01
Application Number : 17533
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : No
TE Code :
Brand Name : KLONOPIN
Dosage Form : TABLET;ORAL
Dosage Strength : 0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-04-09
Application Number : 17533
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : KLONOPIN
Dosage Form : TABLET;ORAL
Dosage Strength : 0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-04-09
Application Number : 17533
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : KLONOPIN RAPIDLY DISINTEGRATING
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-12-23
Application Number : 20813
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KLONOPIN RAPIDLY DISINTEGRATING
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-12-23
Application Number : 20813
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KLONOPIN RAPIDLY DISINTEGRATING
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 0.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-12-23
Application Number : 20813
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KLONOPIN RAPIDLY DISINTEGRATING
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-12-23
Application Number : 20813
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : KLONOPIN RAPIDLY DISINTEGRATING
Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL
Dosage Strength : 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1997-12-23
Application Number : 20813
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
