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01 1ALFUZOSIN HYDROCHLORIDE
02 2ALLOPURINOL
03 1AMIODARONE HYDROCHLORIDE
04 6AMITRIPTYLINE HYDROCHLORIDE
05 3AMLODIPINE BESYLATE
06 3APREMILAST
07 6ARIPIPRAZOLE
08 3ATENOLOL
09 2ATENOLOL; CHLORTHALIDONE
10 1ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE
11 2Amlodipine besilate
12 2Amlodipine besylate
13 2Amoxicillin
14 3Amoxycillin
15 6Ampicillin sodium
16 6Aripiprazole
17 3BACLOFEN
18 2BISOPROLOL FUMARATE
19 3BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE
20 4BUSPIRONE HYDROCHLORIDE
21 4Bisoprolol Fumarate
22 1CARBAMAZEPINE
23 4CELECOXIB
24 4CETIRIZINE HYDROCHLORIDE
25 1CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
26 2CHLORTHALIDONE
27 3CLONIDINE HYDROCHLORIDE
28 3CYCLOBENZAPRINE HYDROCHLORIDE
29 2Cetirizine hydrochloride
30 2Clavulanic acid
31 6Cloxacillin sodium equivalent to cloxacillin anhydrous
32 2DIVALPROEX SODIUM
33 4DONEPEZIL HYDROCHLORIDE
34 4DOXAZOSIN MESYLATE
35 2Donepezil Hydrochloride
36 3ETODOLAC
37 1FAMOTIDINE
38 1Fluoxetine hydrochloride
39 6GUANFACINE HYDROCHLORIDE
40 4HYDROCHLOROTHIAZIDE
41 2HYDROCHLOROTHIAZIDE; IRBESARTAN
42 3HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
43 3IRBESARTAN
44 1KETOTIFEN FUMARATE
45 3LABETALOL HYDROCHLORIDE
46 4LACOSAMIDE
47 3LOSARTAN POTASSIUM
48 4Lamotrigine
49 2Levocetirizine Dihydrochloride
50 1Losartan Potassium
51 2MELOXICAM
52 2MEMANTINE HYDROCHLORIDE
53 2METFORMIN HYDROCHLORIDE
54 2METHSCOPOLAMINE BROMIDE
55 3METOLAZONE
56 2METRONIDAZOLE
57 3MONTELUKAST SODIUM
58 2Meloxicam
59 2Memantine Hydrochloride
60 4NEBIVOLOL HYDROCHLORIDE
61 1ORPHENADRINE CITRATE
62 1PHENYTOIN SODIUM
63 2PINDOLOL
64 2PIROXICAM
65 6PRAMIPEXOLE DIHYDROCHLORIDE
66 2PRASUGREL HYDROCHLORIDE
67 8PREGABALIN
68 1PRIMAQUINE PHOSPHATE
69 1Paracetamol
70 11QUETIAPINE FUMARATE
71 2RANOLAZINE
72 4RIZATRIPTAN BENZOATE
73 2SOLIFENACIN SUCCINATE
74 2Sildenafil Citrate
75 4TADALAFIL
76 4TOLTERODINE TARTRATE
77 1TRAMADOL HYDROCHLORIDE
78 5Tramadol hydrochloride
79 4VALSARTAN
80 2ZALEPLON
81 3ZONISAMIDE
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01 181UNICHEM
02 57Unichem SA (Pty) Ltd
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01 6CAP
02 2CAPSULE, EXTENDED RELEASE;ORAL
03 21CAPSULE;ORAL
04 14FCT
05 1FOR SUSPENSION;ORAL
06 14INJ
07 1SOLUTION/DROPS;OPHTHALMIC
08 23TAB
09 2TABLET, CHEWABLE;ORAL
10 21TABLET, EXTENDED RELEASE;ORAL
11 4TABLET, ORALLY DISINTEGRATING;ORAL
12 129TABLET;ORAL
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01 10.025MG;2.5MG
02 10.125MG
03 10.1MG
04 10.25MG
05 10.2MG
06 10.3MG
07 10.5MG
08 10.75MG
09 11.5MG
10 10100MG
11 1100MG EXTENDED
12 1100MG;25MG
13 2100mg
14 1100mg/2 ml
15 1910MG
16 110MG;6.25MG
17 1110mg
18 212.5MG
19 112.5MG;100MG
20 112.5MG;150MG
21 112.5MG;300MG
22 112.5MG;50MG
23 2125mg
24 4125mg/7.5 ml
25 4150MG
26 315MG
27 315mg
28 1160MG
29 11GM
30 21MG
31 32.5MG
32 12.5MG;6.25MG
33 6200MG
34 1200mg
35 520MG
36 120mg
37 1225MG
38 1250MG
39 2250mg
40 4250mg/7.5 ml
41 725MG
42 125MG;100MG
43 125mg
44 32MG
45 4300MG
46 330MG
47 1320MG
48 237.5mg
49 2400MG
50 140MG
51 140MG/5ML
52 14MG
53 4500MG
54 3500mg
55 4500mg/10 ml
56 1050MG
57 150MG;25MG
58 550mg
59 150mg/ml
60 165MG
61 15MG;120MG
62 15MG;6.25MG
63 95mg
64 1600MG
65 27.5MG
66 17.5mg
67 1750MG
68 375MG
69 180MG
70 1EQ 0.025% BASE
71 1EQ 100MG BASE
72 6EQ 10MG BASE
73 1EQ 150MG BASE
74 1EQ 15MG BASE
75 3EQ 1MG BASE
76 2EQ 2.5MG BASE
77 2EQ 200MG BASE
78 1EQ 20MG BASE
79 1EQ 250MG VALPROIC ACID
80 1EQ 25MG BASE
81 3EQ 2MG BASE
82 2EQ 300MG BASE
83 1EQ 3MG BASE
84 2EQ 400MG BASE
85 3EQ 4MG BASE
86 1EQ 500MG VALPROIC ACID
87 2EQ 50MG BASE
88 6EQ 5MG BASE
89 1EQ 8MG BASE
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01 57South Africa
02 181USA
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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET, EXTENDED RELEASE...
Brand Name : ALFUZOSIN HYDROCHLORIDE
Dosage Strength : 10MG
Packaging :
Approval Date : 2016-01-28
Application Number : 203192
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : ALLOPURINOL
Dosage Strength : 100MG
Packaging :
Approval Date : 2019-03-12
Application Number : 211820
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : ALLOPURINOL
Dosage Strength : 300MG
Packaging :
Approval Date : 2019-03-12
Application Number : 211820
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : AMIODARONE HYDROCHLORIDE
Dosage Strength : 200MG
Packaging :
Approval Date : 2020-07-21
Application Number : 213446
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 10MG
Packaging :
Approval Date : 2021-05-19
Application Number : 214548
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 25MG
Packaging :
Approval Date : 2021-05-19
Application Number : 214548
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 50MG
Packaging :
Approval Date : 2021-05-19
Application Number : 214548
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 75MG
Packaging :
Approval Date : 2021-05-19
Application Number : 214548
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 100MG
Packaging :
Approval Date : 2021-05-19
Application Number : 214548
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Unichem Pharmaceuticals USA, Inc
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 150MG
Packaging :
Approval Date : 2021-05-19
Application Number : 214548
Regulatory Info : RX
Registration Country : USA
