| Denumire comercială | DCI | Forma farmaceutică | Cod ATC | Cod CIM | Firma / țara deținătoare APP |  |
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| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873013 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873014 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873015 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873016 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873017 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873018 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873019 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873020 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873021 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMLODIPINA/VALSARTAN STADA 5 mg/80 mg | COMBINATII (AMLODIPINUM+VALSARTANUM) | COMPR. FILM. | C09DB01 | W62873022 | STADA M&D S.R.L. - ROMANIA | ||||||
| AMMONAPS 500mg | NATRII PHENYLBUTYRATE | COMPR. | A16AX03 | W66278001 | IMMEDICA PHARMA AB - SUEDIA | X | |||||
| AMMONAPS 500mg | NATRII PHENYLBUTYRATE | COMPR. | A16AX03 | W66278002 | IMMEDICA PHARMA AB - SUEDIA | X | |||||
| AMMONAPS 940mg/g | NATRII PHENYLBUTYRATE | GRAN. ORALE | A16AX03 | W66279001 | IMMEDICA PHARMA AB - SUEDIA | X | |||||
| AMMONAPS 940mg/g | NATRII PHENYLBUTYRATE | GRAN. ORALE | A16AX03 | W66279002 | IMMEDICA PHARMA AB - SUEDIA | X | |||||
| AMOKSIKLAV 156,25mg/5ml | AMOXICILLINUM + ACIDUM CLAVULANICUM | PULB. PT. SUSP. ORALA | J01CR02 | W00399002 | LEK PHARMACEUTICALS D.D. - SLOVENIA | ||||||
| AMOKSIKLAV 312,5mg/5ml | AMOXICILLINUM + ACIDUM CLAVULANICUM | PULB. PT. SUSP. ORALA | J01CR02 | W00402002 | LEK PHARMACEUTICALS D.D. - SLOVENIA | ||||||
| AMOKSIKLAV 312,5mg/5ml | AMOXICILLINUM + ACIDUM CLAVULANICUM | PULB. PT. SUSP. ORALA | J01CR02 | W00402003 | LEK PHARMACEUTICALS D.D. - SLOVENIA | ||||||
| AMOKSIKLAV 400 mg/57 mg/5 ml | AMOXICILLINUM + ACIDUM CLAVULANICUM | PULB. PT. SUSP. ORALA | J01CR02 | W08783001 | LEK PHARMACEUTICALS D.D. - SLOVENIA | ||||||
| AMOKSIKLAV 400 mg/57 mg/5 ml | AMOXICILLINUM + ACIDUM CLAVULANICUM | PULB. PT. SUSP. ORALA | J01CR02 | W08783002 | LEK PHARMACEUTICALS D.D. - SLOVENIA | ||||||
| AMOKSIKLAV 400 mg/57 mg/5 ml | AMOXICILLINUM + ACIDUM CLAVULANICUM | PULB. PT. SUSP. ORALA | J01CR02 | W08783003 | LEK PHARMACEUTICALS D.D. - SLOVENIA |
ANMDMR - Nomenclatorul medicamentelor pentru uz uman