01 6ACCORD HLTHCARE
02 6AIPING PHARM INC
03 4AM THERAP
04 2ANDA REPOSITORY
05 4ANI PHARMS
06 1ANI PHARMS INC
07 7ASTRAZENECA
08 6AUROBINDO PHARMA USA
09 5BRISTOL MYERS SQUIBB
10 6CENTAUR PHARMS PVT
11 8CHARTWELL RX
12 6COPLEY PHARM
13 6ENDO OPERATIONS
14 5FOSUN PHARMA
15 6HALSEY
16 2HERITAGE PHARMA
17 5IVAX SUB TEVA PHARMS
18 11LEDERLE
19 6MANKIND PHARMA
20 2MICRO LABS
21 8MUTUAL PHARM
22 15MYLAN
23 2MYLAN PHARMS INC
24 5NEW RIVER
25 11PAR PHARM
26 6PLIVA
27 10PUREPAC PHARM
28 6RISING PHARMA
29 7ROCHE
30 12ROXANE
31 6RUBICON
32 7SANDOZ
33 4SCHERING
34 12SUN PHARM INDS INC
35 4SUN PHARM INDUSTRIES
36 5SUPERPHARM
37 7TEVA
38 6UCB INC
39 6UNICHEM
40 3USL PHARMA
41 4VANGARD
42 6WARNER CHILCOTT
43 24WATSON LABS
44 2WEST WARD
45 6ZYDUS PHARMS
01 1CONCENTRATE;ORAL
02 2INJECTABLE;INJECTION
03 10TABLET; ORAL
04 275TABLET;ORAL
01 205DISCN
02 69RX
03 14Blank
01 5AMITID
02 6AMITRIL
03 196AMITRIPTYLINE HYDROCHLORIDE
04 13CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE
05 7ELAVIL
06 7ENDEP
07 1ETRAFON 2-10
08 1ETRAFON 2-25
09 1ETRAFON-A
10 1ETRAFON-FORTE
11 1LIMBITROL
12 1LIMBITROL DS
13 43PERPHENAZINE AND AMITRIPTYLINE HYDROCHLORIDE
14 1TRIAVIL 2-10
15 1TRIAVIL 2-25
16 1TRIAVIL 4-10
17 1TRIAVIL 4-25
18 1TRIAVIL 4-50
01 259No
02 15Yes
03 14Blank
RLD : Yes
TE Code :
Brand Name : ELAVIL
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Dosage Strength : 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 : 12703
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12703
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12703
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12703
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12703
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : ELAVIL
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 12703
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : ELAVIL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/ML
Approval Date : 1982-01-01
Application Number : 12704
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : ETRAFON-A
Dosage Form : TABLET;ORAL
Dosage Strength : 10MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 14713
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : ETRAFON 2-25
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 14713
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Brand Name : ETRAFON-FORTE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 14713
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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