Unregister. Meropidel®

July 12, 2017
Active substances:
Trade names:
ICD-10:
I.A30-A49.A39    Meningococcal infection
I.A30-A49.A41    Other septicemia
I.A30-A49.A40    Streptococcal septicemia
VI.G00-G09.G00    Bacterial meningitis, not elsewhere classified
X.J10-J18.J15    Bacterial pneumonia, not elsewhere classified
X.J40-J47.J42    Chronic bronchitis, unspecified
XI.K65-K67.K65.0    Acute peritonitis
XII.L00-L08.L01    Impetigo
XII.L00-L08.L02    Abscess of skin, boil and carbuncle
XII.L00-L08.L08.0    Pyoderma
XIV.N10-N16.N11    Chronic tubulointerstitial nephritis
XIV.N10-N16.N10    Acute tubulointerstitial nephritis
XIV.N10-N16.N15.1    Abscess of kidney and adrenal tissue
XIV.N30-N39.N30    Cystitis
XIV.N30-N39.N34    Urethritis and urethral syndrome
XIV.N70-N77.N70    Salpingitis and oophoritis
XIV.N70-N77.N71    Inflammatory diseases of the uterus, except the cervix
XIV.N70-N77.N72    Inflammatory disease of the cervix
XIV.N70-N77.N73.0    Acute parametritis and pelvic cellulite
Meropidel, meropenem, antibiotic carbapenem, treatment of severe infectious and inflammatory diseases, meningitis, sepsis, pneumonia, urinary tract infections, skin and soft tissue infections

The Ministry of Health of the Russian Federation, in accordance with Article 32 of Federal Law No. 61-FZ of 12.04.2010 "On circulation of medicines", decided to abolish state registration and exclude from the state register of medicinal products for medical use of the medicinal product (registration certificate LP-002459 dated 05/05/2014 issued to GlaxoSmithKline Trading, Russia):

Meropidel® (trade name of the medicinal product)

Meropenem (international non-proprietary or grouping or chemical name)

powder for the preparation of a solution for intravenous administration, 500 mg, 1000 mg (dosage form, dosage)

Agila Espelidades Pharmaceuticals LTD, Brazil Estrada Dr. Lourival Martins Beda № 1118, BAIRRO: Donana-Campos, dos Govtacazes, Rio De Janeiro (name and address of the location of the manufacturer of the medicinal product)

on the basis of a filing by an authorized legal entity of ZAO GlaxoSmithKline Trading, an application for the cancellation of the state registration of a medicinal product.