01 2ACETAMINOPHEN; CODEINE PHOSPHATE
02 4AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
03 1ASPIRIN; BUTALBITAL; CAFFEINE
04 2ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
05 1CARISOPRODOL
06 2CEFUROXIME AXETIL
07 1CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
08 3CITALOPRAM HYDROBROMIDE
09 1DICYCLOMINE HYDROCHLORIDE
10 4DIPHENHYDRAMINE HYDROCHLORIDE
11 3ESTRADIOL VALERATE
12 1FLUOXETINE HYDROCHLORIDE
13 4GUANFACINE HYDROCHLORIDE
14 1HALOPERIDOL LACTATE
15 2LEFLUNOMIDE
16 4LEVETIRACETAM
17 4METFORMIN HYDROCHLORIDE, SITAGLIPTIN
18 4METRONIDAZOLE
19 2MYCOPHENOLATE SODIUM
20 2NAPROXEN
21 3PEMOLINE
22 1PHENYLBUTAZONE
23 1PREDNISOLONE
24 1PROPRANOLOL HYDROCHLORIDE
25 2SULFAMETHOXAZOLE; TRIMETHOPRIM
26 3SUMATRIPTAN SUCCINATE
27 4SUNITINIB MALATE
28 2TRIAMCINOLONE DIACETATE
01 8CAPSULE;ORAL
02 8INJECTABLE;INJECTION
03 4TABLET, DELAYED RELEASE;ORAL
04 4TABLET, EXTENDED RELEASE
05 5TABLET, EXTENDED RELEASE;ORAL
06 36TABLET;ORAL
01 20.025MG;2.5MG
02 11000MG
03 1100MG
04 110MG
05 210MG/ML
06 110MG;2MG
07 110MG;4MG
08 118.75MG
09 11GM
10 11MG/ML
11 120MG
12 120MG/ML
13 1212.6MG;EQ 287.5MG BASE
14 3250MG
15 225MG
16 125MG/ML
17 125MG;2MG
18 125MG;4MG
19 1300MG;30MG
20 1300MG;60MG
21 1325MG;50MG;40MG
22 1350MG
23 137.5MG
24 1375MG
25 1400MG;80MG
26 140MG/ML
27 140MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
28 5500MG
29 350MG
30 15MG
31 1750MG
32 175MG
33 1800MG;160MG
34 1EQ 100MG BASE
35 1EQ 100MG BASE TABLET
36 2EQ 10MG BASE
37 1EQ 12.5MG BASE
38 1EQ 180MG BASE
39 1EQ 1MG BASE
40 1EQ 20MG BASE
41 1EQ 250MG BASE
42 2EQ 25MG BASE
43 1EQ 2MG BASE
44 1EQ 360MG BASE
45 1EQ 37.5MG BASE
46 1EQ 3MG BASE
47 1EQ 40MG BASE
48 1EQ 4MG BASE
49 1EQ 500MG BASE
50 2EQ 50MG BASE
51 1EQ 5MG BASE/ML
01 47DISCN
02 14RX
03 4Blank
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 300MG;60MG
Approval Date : 1992-07-16
Application Number : 81249
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET; ORAL
Proprietary Name : ACETAMINOPHEN AND CODEIN...
Dosage Strength : 300MG;30MG
Approval Date : 1992-07-16
Application Number : 81250
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 10MG;2MG
Approval Date : 1987-11-27
Application Number : 71062
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 25MG;2MG
Approval Date : 1987-11-27
Application Number : 71063
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 25MG;4MG
Approval Date : 1987-11-27
Application Number : 71064
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET; ORAL
Proprietary Name : PERPHENAZINE AND AMITRIP...
Dosage Strength : 10MG;4MG
Approval Date : 1987-12-21
Application Number : 71862
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BUTALBITAL, ASPIRIN AND ...
Dosage Strength : 325MG;50MG;40MG
Approval Date : 1984-04-06
Application Number : 86398
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : LONOX
Dosage Strength : 0.025MG;2.5MG
Approval Date : 1982-01-01
Application Number : 85311
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Proprietary Name : DIPHENOXYLATE HYDROCHLOR...
Dosage Strength : 0.025MG;2.5MG
Approval Date : 1982-01-01
Application Number : 86173
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AA
Dosage Form : TABLET; ORAL
Proprietary Name : CARISOPRODOL
Dosage Strength : 350MG
Approval Date : 1989-04-13
Application Number : 81025
RX/OTC/DISCN : RX
RLD : No
TE Code : AA
