01 3ACTAVIS LABS FL INC
02 2AIPING PHARM INC
03 2ANDA REPOSITORY
04 2APOTEX
05 2AUROBINDO PHARMA
06 3CHARTWELL RX
07 2INVAGEN PHARMS
08 2JANSSEN RES AND DEV
09 3JUBILANT CADISTA
10 2KVK TECH
11 2MACLEODS PHARMS LTD
12 2NOVAST LABS
13 2OXFORD PHARMS
14 2PAR PHARM INC
15 1PLIVA
16 2PRINSTON INC
17 6RISING
18 3RUBICON RESEARCH
19 1SANDOZ
20 3SUN PHARM INDS LTD
21 2TEVA PHARMS INTL
22 1TONIX
23 2TWI PHARMS INC
24 3UNICHEM
25 2WATSON LABS
01 2CAPSULE, EXTENDED RELEASE; ORAL
02 10CAPSULE, EXTENDED RELEASE;ORAL
03 44TABLET;ORAL
04 1TABLET;SUBLINGUAL
01 13DISCN
02 42RX
03 2Blank
01 2AMRIX
02 52CYCLOBENZAPRINE HYDROCHLORIDE
03 2FLEXERIL
04 1TONMYA
01 50No
02 5Yes
03 2Blank
RLD : No
TE Code : AB
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1989-05-03
Application Number : 71611
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2006-02-03
Application Number : 71611
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 7.5MG
Approval Date : 2006-02-03
Application Number : 71611
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code :
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1991-11-27
Application Number : 73143
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG
Approval Date : 1991-11-19
Application Number : 72854
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Approval Date : 2006-02-03
Application Number : 72854
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : FLEXERIL
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17821
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : FLEXERIL
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17821
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : AMRIX
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 15MG
Approval Date : 2007-02-01
Application Number : 21777
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : AMRIX
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 30MG
Approval Date : 2007-02-01
Application Number : 21777
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
