01 1ACETAMINOPHEN; BUTALBITAL; CAFFEINE
02 5AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
03 2DEXTROAMPHETAMINE SULFATE
04 6DOXEPIN HYDROCHLORIDE
05 1FERRIC OXYHYDROXIDE
06 2FURAZOLIDONE
07 3HISTRELIN ACETATE
08 1HYDROFLUMETHIAZIDE
09 2HYDROFLUMETHIAZIDE; RESERPINE
10 1IDURSULFASE
11 5LEVODOPA
12 1METHANTHELINE BROMIDE
13 3MORICIZINE HYDROCHLORIDE
14 3NITROFURAZONE
15 7PHENDIMETRAZINE TARTRATE
16 1PHENTERMINE HYDROCHLORIDE
17 2PROPANTHELINE BROMIDE
18 1TETRACYCLINE HYDROCHLORIDE
19 1URACIL MUSTARD
20 2VELAGLUCERASE ALFA
01 1CAPSULE, EXTENDED RELEASE;ORAL
02 13CAPSULE;ORAL
03 1CREAM;TOPICAL
04 1FOR SOLUTION;TOPICAL
05 1INJECTABLE; IV (INFUSION)
06 4INJECTABLE;INJECTION
07 1INJECTABLE;INTRAVENOUS
08 1OINTMENT;TOPICAL
09 1POWDER;INTRAVENOUS
10 1POWDER;TOPICAL
11 1SUSPENSION;ORAL
12 24TABLET;ORAL
01 30.2%
02 2100MG
03 1105MG
04 110MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
05 110MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
06 110MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
07 115MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
08 11MG
09 12.2MG/ML
10 1200 UNITS/VIAL
11 1200MG
12 3250MG
13 125MG;0.125MG
14 125MG;2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
15 125MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
16 1300MG
17 130MG
18 1325MG;50MG;40MG
19 635MG
20 1400 UNITS/VIAL
21 2500MG
22 250MG
23 150MG/15ML
24 150MG;0.125MG
25 150MG;4MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
26 15MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
27 16MG/3ML
28 17.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 1EQ 0.2MG BASE/ML
30 1EQ 0.5MG BASE/ML
31 1EQ 100MG BASE
32 1EQ 10MG BASE
33 1EQ 150MG BASE
34 1EQ 1MG BASE/ML
35 1EQ 25MG BASE
36 1EQ 50MG BASE
37 1EQ 50MG IRON/ML
38 1EQ 75MG BASE
01 47DISCN
02 3Blank
RLD : No
TE Code :
ACETAMINOPHEN; BUTALBITAL; CAFFEINE
Dosage Form : CAPSULE; ORAL
Proprietary Name : ANOQUAN
Dosage Strength : 325MG;50MG;40MG
Approval Date : 1986-10-01
Application Number : 87628
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : TRIAVIL 2-25
Dosage Strength : 25MG;2MG **Federal Regis...
Approval Date : 1982-01-01
Application Number : 14715
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : TRIAVIL 4-10
Dosage Strength : 10MG;4MG **Federal Regis...
Approval Date : 1982-01-01
Application Number : 14715
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : TRIAVIL 2-10
Dosage Strength : 10MG;2MG **Federal Regis...
Approval Date : 1982-01-01
Application Number : 14715
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : TRIAVIL 4-25
Dosage Strength : 25MG;4MG **Federal Regis...
Approval Date : 1982-01-01
Application Number : 14715
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : TRIAVIL 4-50
Dosage Strength : 50MG;4MG **Federal Regis...
Approval Date : 1982-01-01
Application Number : 14715
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROSTAT
Dosage Strength : 5MG **Federal Register d...
Approval Date : 1982-01-01
Application Number : 84051
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : DEXTROSTAT
Dosage Strength : 10MG **Federal Register ...
Approval Date : 1982-01-01
Application Number : 84051
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : DOXEPIN HYDROCHLORIDE
Dosage Strength : EQ 10MG BASE
Approval Date : 1982-01-01
Application Number : 16987
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : DOXEPIN HYDROCHLORIDE
Dosage Strength : EQ 25MG BASE
Approval Date : 1982-01-01
Application Number : 16987
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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