01 2ACETAMINOPHEN; CODEINE PHOSPHATE
02 4AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
03 4APIXABAN
04 1ASPIRIN; BUTALBITAL; CAFFEINE
05 2ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
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 2SITAGLIPTIN PHOSPHATE
25 2SULFAMETHOXAZOLE; TRIMETHOPRIM
26 3SUMATRIPTAN SUCCINATE
27 4SUNITINIB MALATE
28 2TRIAMCINOLONE DIACETATE
01 8CAPSULE;ORAL
02 7INJECTABLE;INJECTION
03 6TABLET
04 4TABLET, DELAYED RELEASE;ORAL
05 4TABLET, EXTENDED RELEASE
06 5TABLET, EXTENDED RELEASE;ORAL
07 35TABLET;ORAL
01 20.025MG;2.5MG
02 11.5MG
03 11000MG
04 2100MG
05 110MG
06 210MG/ML
07 110MG;2MG
08 110MG;4MG
09 118.75MG
10 11GM
11 12.0MG
12 12.5MG
13 120MG
14 120MG/ML
15 1212.6MG;EQ 287.5MG BASE
16 3250MG
17 225MG
18 125MG/ML
19 125MG;2MG
20 125MG;4MG
21 1300MG;30MG
22 1300MG;60MG
23 1325MG;50MG;40MG
24 137.5MG
25 1375MG
26 1400MG;80MG
27 140MG/ML
28 140MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
29 5500MG
30 450MG
31 25MG
32 1750MG
33 175MG
34 1800MG;160MG
35 1EQ 100MG BASE
36 1EQ 100MG BASE TABLET
37 2EQ 10MG BASE
38 1EQ 12.5MG BASE
39 1EQ 180MG BASE
40 1EQ 1MG BASE
41 1EQ 20MG BASE
42 1EQ 250MG BASE
43 2EQ 25MG BASE
44 1EQ 2MG BASE
45 1EQ 360MG BASE
46 1EQ 37.5MG BASE
47 1EQ 3MG BASE
48 1EQ 40MG BASE
49 1EQ 4MG BASE
50 1EQ 500MG BASE
51 2EQ 50MG BASE
52 1EQ 5MG BASE/ML
01 46DISCN
02 13RX
03 10Blank
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 :
TE Code :
Dosage Form : TABLET
Proprietary Name : APIXABAN
Dosage Strength : 1.5MG
Approval Date :
Application Number : 218519
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : TABLET
Proprietary Name : APIXABAN
Dosage Strength : 2.0MG
Approval Date :
Application Number : 218519
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : TABLET
Proprietary Name : APIXABAN
Dosage Strength : 5MG
Approval Date :
Application Number : 218519
RX/OTC/DISCN :
RLD :
TE Code :
RLD :
TE Code :
Dosage Form : TABLET
Proprietary Name : APIXABAN
Dosage Strength : 2.5MG
Approval Date :
Application Number : 218519
RX/OTC/DISCN :
RLD :
TE Code :
