|
UNIDROL 10
Alfuzosin Hydrochloride 10 mg/6 mL,Colloidal Silicon Dioxide (Aerosil-200) 3.000 mg/6 mL,Hydroxypropyl Methyl Cellulose 6 cps 160.000 mg/6 mL,Hypromellose 2910 5CPS, (Methocel E5LV premium) 50.000 mg/6 mL,Lactose Monohydrate (Spray dried) 50.000 mg/6 mL,Magnesium Stearate 3.000 mg/6 mL,Povidone K 29/32 (Plasdone K-29/32 24.000 mg/6 mL,Purified Water q.s. ml
|
Extended Release Tablet
10
|
Tanzania
|
TAN 25 HM 0379
|
Registered/Compliant
|
|
UNIDROL 10
-
|
EXTENDED RELEASE TABLETS
|
Botswana
|
BOT2304046
|
Registered/Compliant
|
|
UNIDROL 10
ALFUZOSIN HYDROCHLORIDE
|
TABLET; ORAL
10MG
|
Zimbabwe
|
2024/21.7/6641
|
PRESCRIPTION PREPARATIONS 10TH SCHEDULE, (P.P.10)
|
|
UNIENZYME CMPS
CHARCOAL ACTIVATED; DIASTASE; NICOTINAMIDE; PAPAIN; SIMETHICONE
|
TABLET, COATED; ORAL
50/75/25/30/20MG16.8
|
Zimbabwe
|
2025/16.8.2/6818
|
PHARMACY MEDICINES (P.)
|
|
UNIENZYME TABLETS (Each tablet contains Fungal Diastase (1:800)/ Papain / Simethicone / Activated Charcoal / Nicotinamide -20mg/30mg/50mg/75mg/25mg)
Fungal Diastase (1:800)/ Papain / Simethicone / Activated Charcoal / Nicotinamide
|
TABLETS
20mg/30mg/50mg/75mg/25mg
|
Ghana
|
FDA/SD.243-010068
|
3 months to expiry
|
|
UNIFEN 10
Baclofen 10 mg/6 mL,Colloidal Silicon Dioxide (Aerosil-200) 1.500 mg/6 mL,Magnesium stearate (vegetable) 0.750 mg/6 mL,Microcrystalline cellulose (Avicel PH102) 85.250 mg/6 mL,Povidone K-29/32 2.500 mg/6 mL,Pregelatinised Starch (Starch 1500) 40.000 mg/6 mL
|
Oral tablet
10
|
Tanzania
|
TAN 25 HM 0579
|
Registered/Compliant
|
|
UNIFEN 20
Baclofen 20 mg/6 mL,Colloidal Silicon Dioxide (Aerosil-200) 3.000 mg/6 mL,Magnesium stearate (vegetable) 1.500 mg/6 mL,Microcrystalline cellulose (Avicel PH102) 170.500 mg/6 mL,Povidone K-29/32 5.000 mg/6 mL,Pregelatinised Starch (Starch 1500) 80.000 mg/6 mL
|
Oral tablet
20
|
Tanzania
|
TAN 25 HM 0645
|
Registered/Compliant
|
|
UNIPROEX ER 250
Colloidal Silicon dioxide (Aerosil® 200 Pharma) 21.000 mg/6 mL,Divalproex Sodium equivalent to Divalproex 250 mg/6 mL,Ethylcellulose 10 mPa.s 12.500 mg/6 mL,Ethylcellulose 10 mPa.s 5.000 mg/6 mL,Hypromellose 2208 – 15000 mPa.s 165.000 mg/6 mL,Isopropyl Alcohol* q.s. mg/6 mL,Lactose Monohydrate (Pharmatose 200M Lactose) 8.439 mg/6 mL,Opacode Black S-1-277001 q.s. mg,Opadry II 32K540052 Pink 12.500 mg,Purified Water q.s. mg/6 mL,Stearic Acid 1.500 mg,Talc 1.000 mg
|
Extended Release Tablet
|
Tanzania
|
TAN 22 HM 0508
|
Registered/Compliant
|
|
UNIPROEX ER 250
-
|
EXTENDED- RELEASE TABLETS
|
Botswana
|
BOT2404160
|
Registered/Compliant
|
|
UNIPROEX ER 250
-
|
EXTENDED- RELEASE TABLETS
|
Botswana
|
BOT2404160A
|
Registered/Compliant
|
|
UNIPROEX ER 250
DIVALPROEX SODIUM
|
TABLET, COATED; ORAL
250MG
|
Zimbabwe
|
2024/13.1/6607
|
PRESCRIPTION PREPARATIONS 9TH SCHEDULE, (P.P.)
|
|
UNIPROEX ER 500
Colloidal Silicon dioxide (Aerosil 200) - IN ACTIVE TABLETS 42.00 mg/6 mL,Divalproex Sodium equivalent to Divalproex 500 mg/6 mL,Ethylcellulose 10 mPa.s 10.000 mg/6 mL,Ethylcellulose 10 mPa.s 25.000 mg/6 mL,Hypromellose 2208 – 15000 mPa.s 330.00 mg/6 mL,Isopropyl Alcohol q.s. mg,Isopropyl Alcohol q.s. mg/6 mL,Lactose Monohydrate (Pharmatose 200M Lactose) 16.878 mg/6 mL,Opacode Black S-1-277001 q.s. mg/6 mL,Opadry II 32K520138 (Yellow) 25.000 mg/6 mL,Purified Water q.s. mg,Purified Water q.s. mg/6 mL,Stearic Acid 3.000 mg/6 mL,Talc 2.000 mg/6 mL
|
Extended Release Tablet
|
Tanzania
|
TAN 22 HM 0509
|
Registered/Compliant
|
|
UNIPROEX ER 500
-
|
EXTENDED- RELEASE TABLETS
|
Botswana
|
BOT2404161
|
Registered/Compliant
|
|
UNIPROEX ER 500
-
|
EXTENDED- RELEASE TABLETS
|
Botswana
|
BOT2404161A
|
Registered/Compliant
|
|
UNIPROEX ER 500
DIVALPROEX SODIUM
|
TABLET, COATED; ORAL
500MG
|
Zimbabwe
|
2024/13.1/6608
|
PRESCRIPTION PREPARATIONS 9TH SCHEDULE, (P.P.)
|
|
UNITROL ER 2
Ethylcellulose Dispersion Type B (Surelease E-7-19040) 40.024 (25% dispersion) (10.006 solid content mg/6 mL,Ethylcellulose Dispersion Type B (Surelease E-7-19040) 45.564 (25% dispersion) (11.391 solid content) mg,Hard Gelatin Capsule of size “4” with light green opaque cap and body imprinted with “U” on cap and “306” on the body with black ink 1 no. (39.000 mg) mg/6 mL,Hypromellose 2910-5 mPa.s (Methocel E5 Premium LV Hydroxypropyl Methyl Cellulose) 1.800 mg/6 mL,Hypromellose 2910-5 mPa.s (Methocel E5 Premium LV Hydroxypropyl Methyl Cellulose) 1.878 mg/6 mL,Purified Water. q.s. q.s,Sugar Spheres Suglets Sugar Spheres PF010 710/850 (20/25 mesh) 68.500 mg,Talc 0.500 mg/6 mL,Tolterodine Tartrate 2 mg
|
Capsules
2
|
Tanzania
|
TAN 25 HM 0271
|
Registered/Compliant
|
|
UNITROL ER 4
Ethylcellulose Dispersion Type B (Surelease E-7-19040) 80.048 (25% dispersion) (20.012 solid content) mg/6 mL,Ethylcellulose Dispersion Type B (Surelease E-7-19040) 91.128 (25% dispersion) (≈22.782 solid content) mg/6 mL,Hard Gelatin Capsule of size “3” with light blue opaque cap and body imprinted with “U” on cap and “307” on the body with black ink 1 Nos,Hypromellose 2910-5 mPa.s (Methocel E5 Premium LV Hydroxypropyl Methyl Cellulose) 3.600 mg/6 mL,Hypromellose 2910-5 mPa.s (Methocel E5 Premium LV Hydroxypropyl Methyl Cellulose) 3.756 mg/6 mL,Purified Water. q.s. q.s,Sugar Spheres Suglets Sugar Spheres PF010 710/850 (20/25 mesh) 137.000 mg/6 mL,Talc 1.000 mg/6 mL,Tolterodine Tartrate 4 mg/6 mL
|
Capsules
4
|
Tanzania
|
TAN 25 HM 0574
|
Registered/Compliant
|
|
Unichlor 50
Chlorthalidone USP 50 mg/6 mL,Colloidal Silicon dioxide (Aerosil 200) - IN ACTIVE TABLETS 0.600 mg/6 mL,D & C yellow No. 10 Lake 0.300 mg/6 mL,Lake pigment HT 5516 FD&C Blue #1 0.120 mg/6 mL,Microcrystalline cellulose (Avicel PH101) 58 mg/6 mL,Pregelatinized Starch (1500 LM) 20.980 mg/6 mL,Purified Water USP-NF/Ph.Eur q.s. mg/6 mL,Sodium starch glicolate (type A) 9.000 mg/6 mL,Stearic Acid - IN ACTIVE TABLETS 1.000 mg/6 mL
|
Tablets
|
Tanzania
|
TAN 23 HM 0573
|
Registered/Compliant
|
|
Unienzyme cMPS
Activated Charcoal 75 mg,Fungal Diastase 20 mg,Nicotinamide 25 mg,Papain 30 mg,Simethicone 50 mg
|
Tablets
|
Tanzania
|
TAN 00,897 A09A UNI
|
Registered/Compliant
|
|
Unienzyme cMPS tablet
Activated Charcoal 75.000 mg,Fungal Diastase (1:800) equivalent to (1:4000) O. sp 20.000 mg,Nicotinamide 25.000 mg,Papain (6000 units/mg) equivalent to (48000 units/mg) 30.000 mg,Simethicone 50.000 mg
|
Tablet Chewable
20.000 mg,25.000 mg,30.000 mg,50.000 mg,75.000 mg
|
Zambia
|
268/020
|
Registered/Compliant
|