01 3ACTAVIS LABS FL INC
02 2AIPING PHARM INC
03 2ANDA REPOSITORY
04 2APOTEX
05 2AUROBINDO PHARMA
06 3CHARTWELL RX
07 3GRAVITI PHARMS
08 2INVAGEN PHARMS
09 2JANSSEN RES AND DEV
10 3JUBILANT CADISTA
11 2KVK TECH
12 2MACLEODS PHARMS LTD
13 2NOVAST LABS
14 2OXFORD PHARMS
15 2PAR PHARM INC
16 1PLIVA
17 2PRINSTON INC
18 3RISING
19 3RUBICON
20 1SANDOZ
21 3SUN PHARM INDS LTD
22 2TEVA PHARMS INTL
23 2TWI PHARMS INC
24 3UNICHEM
25 2WATSON LABS
01 2CAPSULE, EXTENDED RELEASE; ORAL
02 10CAPSULE, EXTENDED RELEASE;ORAL
03 44TABLET;ORAL
01 13DISCN
02 41RX
03 2Blank
01 2AMRIX
02 52CYCLOBENZAPRINE HYDROCHLORIDE
03 2FLEXERIL
01 50No
02 4Yes
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Dosage Strength : 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
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