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 1Daptomycin
12 3ESTRADIOL VALERATE
13 1FLUOXETINE HYDROCHLORIDE
14 4GUANFACINE HYDROCHLORIDE
15 1HALOPERIDOL LACTATE
16 2LEFLUNOMIDE
17 4LEVETIRACETAM
18 4METFORMIN HYDROCHLORIDE, SITAGLIPTIN
19 4METRONIDAZOLE
20 2MYCOPHENOLATE SODIUM
21 2NAPROXEN
22 3PEMOLINE
23 1PHENYLBUTAZONE
24 1PREDNISOLONE
25 1PROPRANOLOL HYDROCHLORIDE
26 2SULFAMETHOXAZOLE; TRIMETHOPRIM
27 3SUMATRIPTAN SUCCINATE
28 4SUNITINIB MALATE
29 2TRIAMCINOLONE DIACETATE
30 1Voriconazole
01 48FOSUN PHARMA
02 13FOSUN WANBANG
03 4FOSUN WANBANG (JIANGSU) PHARMACEUTICAL GROUP CO.,
04 2Fosun Pharma Sp.Z Oo
01 8CAPSULE;ORAL
02 8INJECTABLE;INJECTION
03 1Powder For Injection And Infusion Solution
04 1Powder For Solution For Infusion
05 4TABLET, DELAYED RELEASE;ORAL
06 4TABLET, EXTENDED RELEASE
07 5TABLET, EXTENDED RELEASE;ORAL
08 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 1200MG
12 120MG
13 120MG/ML
14 1212.6MG;EQ 287.5MG BASE
15 3250MG
16 225MG
17 125MG/ML
18 125MG;2MG
19 125MG;4MG
20 1300MG;30MG
21 1300MG;60MG
22 1325MG;50MG;40MG
23 2350MG
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28 140MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 350MG
31 15MG
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 2Spain
02 65USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET;ORAL
Brand Name : ACETAMINOPHEN AND CODEINE...
Dosage Strength : 300MG;60MG
Packaging :
Approval Date : 1992-07-16
Application Number : 81249
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ACETAMINOPHEN; CODEINE PHOSPHATE
Dosage Form : TABLET;ORAL
Brand Name : ACETAMINOPHEN AND CODEINE...
Dosage Strength : 300MG;30MG
Packaging :
Approval Date : 1992-07-16
Application Number : 81250
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET;ORAL
Brand Name : PERPHENAZINE AND AMITRIPT...
Dosage Strength : 10MG;2MG
Packaging :
Approval Date : 1987-11-27
Application Number : 71062
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET;ORAL
Brand Name : PERPHENAZINE AND AMITRIPT...
Dosage Strength : 25MG;2MG
Packaging :
Approval Date : 1987-11-27
Application Number : 71063
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET;ORAL
Brand Name : PERPHENAZINE AND AMITRIPT...
Dosage Strength : 25MG;4MG
Packaging :
Approval Date : 1987-11-27
Application Number : 71064
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE
Dosage Form : TABLET;ORAL
Brand Name : PERPHENAZINE AND AMITRIPT...
Dosage Strength : 10MG;4MG
Packaging :
Approval Date : 1987-12-21
Application Number : 71862
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BUTALBITAL, ASPIRIN AND C...
Dosage Strength : 325MG;50MG;40MG
Packaging :
Approval Date : 1984-04-06
Application Number : 86398
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : LONOX
Dosage Strength : 0.025MG;2.5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 85311
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Brand Name : DIPHENOXYLATE HYDROCHLORI...
Dosage Strength : 0.025MG;2.5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 86173
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CARISOPRODOL
Dosage Strength : 350MG
Packaging :
Approval Date : 1989-04-13
Application Number : 81025
Regulatory Info : RX
Registration Country : USA
