| L04AB04 |
Adalimumab |
Humira |
Solution for injection |
40mg/0.8ml |
|
2 pre-filled syringes + 2 alcohol pads |
AbbVie Ltd, Обединено Кралство |
2.9 |
mg |
- |
1725.38 |
62.53643 |
1725.38 |
75% |
1294.03 |
За експертиза по чл.78 т.2 от ЗЗО |
K50.0,K50.1,K51.0,K51.1,K51.3,K51.5,K51.8,K51.9,L40.0,M05.0,M05.1,M05.3,M05.8,M07.1,M07.2,M07.3,M08.1,M08.3,M08.4,M45.0,M45.1,M45.2,M45.3,M45.4,M45.5,M45.6,M45.7,M45.8 |
№ 41/26.11.2009; № 56/05.03.2010; КЦРР-468/19.04.2012 ; КЦPP-2859/20.03.2013; КЦРР-2819/20.03.2013 г.; НСР-605/23.07.2013; НСР-1072/02.09.2013; Протокол 50/23.01.2014; НСР-2398/21.01.2014; НСР-4440/15.08.2014; НСР-4812/13.10.2014.; НСР-6428/12.06.2015.; НСР-8024/08.02.2016.; НСР-10449/29.09.2016; НСР-14664/20.12.2017; НСР-16148/13.07.2018 |
02.08.2018 |
08.09.2012 |
|
Заличен |
3216 |
| L04AB04 |
Adalimumab |
Humira |
Solution for injection |
40 mg/0.8 ml |
|
2 carton pack (Each carton contains:1 vial +1 syringe +1 needle +1 sterile adapter, 2 alcohol pads) |
AbbVie Deutschland GmbH & Co. KG, Германия |
2.9 |
mg |
- |
1767.54 |
50.01449 |
1379.9 |
75% |
1034.92 |
за експертиза по чл.78, т.2 от ЗЗО; да се прилага при лица до 18 години . |
K50.0,K50.1,L40.0,M08.1,M08.3,M08.4 |
НСР-7034/03.09.2015 и НСР-7083/10.09.2015.; НСР-9120/27.04.2016; КП-138/06.11.2017 и НСР-13550/18.08.2017; НСР-16166/13.07.2018; НСР-16255/27.07.2018; НСР-17403/06.12.2018 |
02.01.2019 |
|
|
Заличен |
4064 |
| L04AB04 |
Adalimumab |
Humira |
Solution for injection |
80mg/0.8ml |
|
1 pre-filled syringe + 1 alcohol pad |
AbbVie Deutschland GmbH & Co. KG, Германия |
2.9 |
mg |
- |
1599.13 |
38.13084 |
1052.03 |
75% |
789.02 |
за експертиза по чл.78 т.2 от ЗЗО |
K50.0,K50.1,K51.0,K51.1,K51.3,K51.5,K51.8,K51.9,L40.0,M05.0,M05.1,M05.3,M05.8 |
НСР-17448/06.12.2018 |
02.04.2019 |
|
|
Активен |
16377 |
| L04AB04 |
Adalimumab |
Hyrimoz |
Solution for injection |
40 mg/0.8 ml |
|
2 pre-filled pens |
Sandoz GmbH, Австрия |
2.9 |
mg |
- |
1052.03 |
38.13084 |
1052.03 |
75% |
789.02 |
За експертиза по чл. 78 т. 2 от ЗЗО |
K50.0,K50.1,K51.0,K51.1,K51.3,K51.5,K51.8,K51.9,L40.0,M05.0,M05.1,M05.3,M05.8,M07.1,M07.2,M07.3,M08.1,M08.3,M08.4,M45.0,M45.1,M45.2,M45.3,M45.4,M45.5,M45.6,M45.7,M45.8 |
НСР-18191/18.03.2019 предварително изпълнение |
02.04.2019 |
|
|
Активен |
16454 |
| L04AB05 |
Certolizumab pegol |
L04AB05 Cetrolizumab |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| L04AB05 |
Certolizumab pegol |
CIMZIA |
Solution for injection |
200 |
mg |
2 pre-filled syringes + 2 alcohol wipes |
UCB Pharma SA, Белгия |
14 |
mg |
- |
1517.23 |
53.10571 |
1517.23 |
75% |
1137.92 |
За експертиза по чл.78 т.2 от ЗЗО |
M05.0,M05.1,M05.3,M05.8,M07.1,M07.2,M07.3,M45.0,M45.1,M45.2,M45.3,M45.4,M45.5,M45.6,M45.7,M45.8 |
№ 180/ 27.07.2011; № 185/ 15.08.2011; КЦРР-899/28.06.2012 г.; Протокол 50/23.01.2014; НСР-2978/12.03.2014; НСР-4638/25.09.2014; НСР-5662/18.02.2015; НСР-7367/05.11.2015; НСР-9623/23.06.2016 г.; НСР-15245/09.03.2018 Предварително изпълнение |
02.04.2018 |
08.09.2012 |
|
Активен |
3583 |
| L04AB06 |
Golimumab |
L04AB06 Golimumab |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| L04AB06 |
Golimumab |
Simponi |
Solution for injection |
50 mg/0,5 ml |
|
1 pre-filled syringe |
Janssen Biologics B.V., Нидерландия |
1.66 |
mg |
- |
1731.96 |
57.50199 |
1731.96 |
75% |
1298.97 |
За експертиза по чл.78 т.2 от ЗЗО |
K51.0,K51.1,K51.3,K51.5,K51.8,K51.9,M05.0,M05.1,M05.3,M05.8,M07.1,M07.2,M07.3,M45.0,M45.1,M45.2,M45.3,M45.4,M45.5,M45.6,M45.7,M45.8 |
№ 201/ 19.10.2011; Протокол 50/23.01.2014; НСР-2349/13.01.2014; НСР-1824/25.11.2013 и КП-49/28.05.2014; НСР-3780/16.06.2014.; НСР-5957/01.04.2015.; НСР-9616/23.06.2016; НСР-12560/05.05.2017; НСР-16439/09.08.2018 |
02.09.2018 |
08.09.2012 |
|
Активен |
3739 |
| L04AB06 |
Golimumab |
SIMPONI |
Solution for injection |
50 |
mg |
pre-filled pen x 1 |
Janssen Biologics B.V., Нидерландия |
1.66 |
mg |
- |
1731.96 |
57.50199 |
1731.96 |
75% |
1298.97 |
За експертиза по чл.78 т.2 от ЗЗО |
K51.0,K51.1,K51.3,K51.5,K51.8,K51.9,M05.0,M05.1,M05.3,M05.8,M07.1,M07.2,M07.3,M45.0,M45.1,M45.2,M45.3,M45.4,M45.5,M45.6,M45.7,M45.8 |
№ 190/ 22.08.2011; № 194/ 23.08.2011; Протокол 50/23.01.2014; НСР-2349/13.01.2014; НСР-140/07.06.2013 и КП-5/05.02.2014; НСР-1565/25.10.2013 и КП-50/28.05.2014; НСР-3780/16.06.2014.; НСР-5958/01.04.2015.; НСР-9615/23.06.2016; НСР-12559/05.05.2017; НСР-16437/09.08.2018 |
02.09.2018 |
08.09.2012 |
|
Активен |
3740 |
| L04AC05 |
Ustekinumab |
L04AC05 Ustekinumab |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| L04AC05 |
Ustekinumab |
STELARA |
Solution for injection |
45 |
mg |
1 pre-filled syringe |
Janssen-Cilag International N.V., Белгия |
0.54 |
mg |
- |
5053.94 |
60.64971 |
5053.94 |
75% |
3790.45 |
За експертиза по чл.78 т.2 от ЗЗО |
L40.0,M07.1,M07.2,M07.3 |
НСР-1117/10.09.2013; НСР-1287/27.09.2013; НСР-3654/29.05.2014; НСР-4437/15.08.2014; НСР-5746/26.02.2015.; НСР-9217/ 05.05.2016; НСР-11559/26.01.2017; НСР-14236/19.10.2017; НСР-16130/13.07.2018 (предварително изпълнение) |
02.08.2018 |
|
|
Активен |
3636 |
| L04AC07 |
Tocilizumab |
L04AC07 Tocilizumab |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| L04AC07 |
Tocilizumab |
RoActemra |
Concentrate for solution for infusion |
20 mg/ml - 4 ml |
mg |
1 |
Roche Registration GmbH, Германия |
20 |
mg |
- |
287.05 |
63.889 |
255.56 |
75% |
191.67 |
експертиза по чл. 78 т.2 от ЗЗО |
M05.0,M05.1,M05.3,M05.8,M08.2,M08.3,M08.4 |
КЦРР-821/15.06.2012 г.; КЦРР-910/28.06.2012 г.; НСР-436/09.07.2013; Протокол 50/23.01.2014; НСР-2941/07.03.2014; НСР-5076/21.11.2014; НСР-10018/18.08.2016; НСР-14456/17.11.2017; НСР-15983/22.06.2018 |
02.08.2018 |
08.09.2012 |
|
Активен |
3376 |
| L04AC07 |
Tocilizumab |
RoActemra |
Concentrate for solution for infusion |
20 mg/ml - 20 ml |
mg |
1 |
Roche Registration GmbH, Германия |
20 |
mg |
- |
1277.78 |
63.889 |
1277.78 |
75% |
958.33 |
експертиза по чл. 78 т.2 от ЗЗО |
M05.0,M05.1,M05.3,M05.8,M08.2,M08.3,M08.4 |
КЦРР-821/15.06.2012 г.; КЦРР-910/28.06.2012 г.; НСР-434/09.07.2013 ; Протокол 50/23.01.2014; НСР-2939/07.03.2014; НСР-5078/21.11.2014; НСР-10019/18.08.2016; НСР-14455/17.11.2017; НСР-15986/22.06.2018 |
02.08.2018 |
08.09.2012 |
|
Активен |
3378 |
| L04AC07 |
Tocilizumab |
RoActemra |
Concentrate for solution for infusion |
20 mg/ml - 10 ml |
mg |
1 |
Roche Registration GmbH, Германия |
20 |
mg |
- |
659.89 |
63.889 |
638.89 |
75% |
479.16 |
експертиза по чл. 78 т.2 от ЗЗО |
M05.0,M05.1,M05.3,M05.8,M08.2,M08.3,M08.4 |
КЦРР-821/15.06.2012 г.; КЦРР-910/28.06.2012 г. ; НСР-435/09.07.2013 ; Протокол 50/23.01.2014; НСР-2940/07.03.2014; НСР-5077/21.11.2014; НСР-13342/28.07.2017; НСР-15987/22.06.2018 |
02.08.2018 |
08.09.2012 |
|
Активен |
3377 |
| L04AC07 |
Tocilizumab |
L04AC07 Tocilizumab |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| L04AC07 |
Tocilizumab |
RoActemra |
Solution for injection |
162 |
mg |
4 pre-filled syringes |
Roche Registration GmbH, Германия |
20 |
mg |
- |
1962.71 |
60.57747 |
1962.71 |
75% |
1472.03 |
експертиза по чл. 78 т.2 от ЗЗО |
M05.0,M05.1,M05.3,M05.8,M08.2,M08.3,M08.4 |
НСР-4826/ 13.10.2014.; НСР-6424/12.06.2015.; НСР-13341/28.07.2017; НСР-15981/22.06.2018; НСР-16899/28.09.2018; НСР-16870/28.09.2018; НСР-17828/30.01.2019 |
02.03.2019 |
|
|
Активен |
3260 |
| L04AC07 |
Tocilizumab |
RoActemra |
Solution for injection |
162 |
mg |
4 pre-filled pens |
Roche Registration GmbH, Германия |
20 |
mg |
- |
2019.37 |
60.57747 |
1962.71 |
75% |
1472.03 |
експертиза по чл. 78 т.2 от ЗЗО |
M05.0,M05.1,M05.3,M05.8 |
НСР-16864/28.09.2018 |
02.11.2018 |
|
|
Активен |
16292 |
| L04AC10 |
Secukinumab |
L04AC10 Secukinumab |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| L04AC10 |
Secukinumab |
Cosentyx |
Solution for injection |
150 mg/ml - 1 ml |
|
2 pre-filled pens |
Novartis Europharm Limited, Ирландия |
10 |
mg |
- |
2426.54 |
80.88467 |
2426.54 |
75% |
1819.9 |
За експертиза по чл.78 т.2 от ЗЗО |
L40.0,M07.1,M07.2,M07.3,M45.0,M45.1,M45.2,M45.3,M45.4,M45.5,M45.6,M45.7,M45.8 |
НСР-11313/22.12.2016 (предварително изпълнение); НСР-15156/02.03.2018; НСР-16297/27.07.2018; НСР-17045/22.10.2018 предварително изпълнение |
02.11.2018 |
|
|
Активен |
15529 |
| L04AC10 |
Secukinumab |
Cosentyx |
Solution for injection |
150 mg/ml-1 ml |
|
1 prefilled pen |
Novartis Europharm Limited, Ирландия |
10 |
mg |
- |
1236.62 |
80.88467 |
1213.27 |
75% |
909.95 |
За експеrтиза по чл.78 т.2 от ЗЗО |
L40.0,M07.1,M07.2,M07.3,M45.0,M45.1,M45.2,M45.3,M45.4,M45.5,M45.6,M45.7,M45.8 |
НСР-14717/20.12.2017; НСР-16298/27.07.2018 |
02.11.2018 |
|
|
Активен |
15986 |
| L04AC13 |
Ixekizumab |
L04AC13 Ixekizumab |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| L04AC13 |
Ixekizumab |
Taltz |
Solution for injection |
80 mg x 1 ml |
|
3 pre-filled pens (single- dose) |
Eli Lilly Nederland B.V, Нидерландия |
2.9 |
mg |
- |
6815.9 |
82.35742 |
6815.9 |
75% |
5111.93 |
за експертиза по чл.78 т.2 от ЗЗО |
L40.0 |
НСР-17655/27.12.2018 предварително изпълнение |
02.01.2019 |
|
|
Активен |
16392 |
| L04AD01 |
Ciclosporin |
L04AD01 Ciclosporin |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| L04AD01 |
Ciclosporin |
Ciclosporin Alkaloid |
Capsule, soft |
100 |
mg |
50 |
Alkaloid – INT d.o.o., Словения |
250 |
mg |
130.01 |
- |
6.053 |
121.06 |
100% |
121.06 |
За експертиза по чл.78 т.2 от ЗЗО |
Z94 |
№ 208/ 04.11.2011; КЦРР-1046/26.07.2012 г.; КЦPP-1147/02.08.2012 г.; КЦРР-2566/14.03.2013 |
04.04.2013 |
08.09.2012 |
|
Заличен |
898 |