| Denumire comercială | DCI | Forma farmaceutică | Cod ATC | Cod CIM | Firma / țara deținătoare APP |  |
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| REVOLADE 25 mg | ELTROMBOPAG | COMPR. FILM. | B02BX05 | W64445001 | NOVARTIS EUROPHARM LIMITED - IRLANDA | X | |||||
| REVOLADE 25 mg | ELTROMBOPAG | COMPR. FILM. | B02BX05 | W64445002 | NOVARTIS EUROPHARM LIMITED - IRLANDA | X | |||||
| REVOLADE 25 mg | ELTROMBOPAG | COMPR. FILM. | B02BX05 | W64445003 | NOVARTIS EUROPHARM LIMITED - IRLANDA | X | |||||
| REVIGRIP SINUS 500 mg/30 mg | COMBINATII (PARACETAMOLUM+PSEUDOEPHEDRINUM) | COMPR. FILM. | N02BE51 | W69427001 | LABORMED PHARMA S.A. - ROMANIA | ||||||
| REVIGRIP SINUS 500 mg/30 mg | COMBINATII (PARACETAMOLUM+PSEUDOEPHEDRINUM) | COMPR. FILM. | N02BE51 | W69427002 | LABORMED PHARMA S.A. - ROMANIA | ||||||
| REVIGRIP HOT LEMON 500 mg/200 mg/10 mg | COMBINATII (PARACETAMOLUM+GUAIFENESINUM+PHENYLEPHRINUM) | PULB. PT. SOL. ORALA | N02BE51 | W66382001 | CHEFARO IRELAND DAC - IRLANDA | ||||||
| REVIGRIP HOT LEMON 500 mg/200 mg/10 mg | COMBINATII (PARACETAMOLUM+GUAIFENESINUM+PHENYLEPHRINUM) | PULB. PT. SOL. ORALA | N02BE51 | W66382002 | CHEFARO IRELAND DAC - IRLANDA | ||||||
| REVIGRIP HOT LEMON 500 mg/200 mg/10 mg | COMBINATII (PARACETAMOLUM+GUAIFENESINUM+PHENYLEPHRINUM) | PULB. PT. SOL. ORALA | N02BE51 | W66382003 | CHEFARO IRELAND DAC - IRLANDA | ||||||
| REVESTIVE | TEDUGLUTIDUM | PULB.+SOLV. PT. SOL. INJ. | A16AX08 | W68911001 | TAKEDA PHARMACEUTICALS INTERNATIONAL AG IRELAND BRANCH - IRLANDA | X | |||||
| REVESTIVE | TEDUGLUTIDUM | PULB.+SOLV. PT. SOL. INJ. | A16AX08 | W68912001 | TAKEDA PHARMACEUTICALS INTERNATIONAL AG IRELAND BRANCH - IRLANDA | X | |||||
| REVESTIVE | TEDUGLUTIDUM | PULB.+SOLV. PT. SOL. INJ. | A16AX08 | W68912002 | TAKEDA PHARMACEUTICALS INTERNATIONAL AG IRELAND BRANCH - IRLANDA | X | |||||
| REVERPLEG 40 U.I./2 ml | VASOPRESINUM (ARGIPRESINUM) | CONC. PT. SOL. PERF. | H01BA01 | W64905001 | ORPHA-DEVEL HANDELS UND VERTRIEBS GMBH - AUSTRIA | ||||||
| REVERPLEG 40 U.I./2 ml | VASOPRESINUM (ARGIPRESINUM) | CONC. PT. SOL. PERF. | H01BA01 | W64905002 | ORPHA-DEVEL HANDELS UND VERTRIEBS GMBH - AUSTRIA | ||||||
| REVERANTZA 40 mg/5 mg | COMBINATII (OLMESARTANUM MEDOXOMILUM+AMLODIPINUM) | COMPR. FILM. | C09DB02 | W67836001 | SWYSSI AG - GERMANIA | ||||||
| REVERANTZA 40 mg/5 mg | COMBINATII (OLMESARTANUM MEDOXOMILUM+AMLODIPINUM) | COMPR. FILM. | C09DB02 | W67836002 | SWYSSI AG - GERMANIA | ||||||
| REVERANTZA 40 mg/5 mg | COMBINATII (OLMESARTANUM MEDOXOMILUM+AMLODIPINUM) | COMPR. FILM. | C09DB02 | W67836003 | SWYSSI AG - GERMANIA | ||||||
| REVERANTZA 40 mg/5 mg | COMBINATII (OLMESARTANUM MEDOXOMILUM+AMLODIPINUM) | COMPR. FILM. | C09DB02 | W67836004 | SWYSSI AG - GERMANIA | ||||||
| REVERANTZA 20 mg/5 mg | COMBINATII (OLMESARTANUM MEDOXOMILUM+AMLODIPINUM) | COMPR. FILM. | C09DB02 | W67835001 | SWYSSI AG - GERMANIA | ||||||
| REVERANTZA 20 mg/5 mg | COMBINATII (OLMESARTANUM MEDOXOMILUM+AMLODIPINUM) | COMPR. FILM. | C09DB02 | W67835002 | SWYSSI AG - GERMANIA | ||||||
| REVERANTZA 20 mg/5 mg | COMBINATII (OLMESARTANUM MEDOXOMILUM+AMLODIPINUM) | COMPR. FILM. | C09DB02 | W67835003 | SWYSSI AG - GERMANIA |
ANMDMR - Nomenclatorul medicamentelor pentru uz uman