Epilim EC New Zealand - English - Medsafe (Medicines Safety Authority)

epilim ec

pharmacy retailing (nz) ltd t/a healthcare logistics - sodium valproate 200mg; sodium valproate 200mg; sodium valproate 200mg - modified release tablet - 200 mg - active: sodium valproate 200mg excipient: calcium silicate citric acid diethyl phthalate hypromellose macrogol 6000 magnesium stearate opaspray violet k-1-4613 polyvinylacetate phthalate povidone purified talc stearic acid active: sodium valproate 200mg excipient: calcium silicate citric acid diethyl phthalate hypromellose macrogol 6000 magnesium stearate opaspray polyvinylacetate phthalate povidone purified talc stearic acid active: sodium valproate 200mg excipient: calcium silicate magnesium stearate povidone purified talc violet enteric coat excipient blend violet sub-coat excipient blend - epilepsy: primary generalised epilepsy (petit mal absences, various forms of myoclonic epilepsy and tonic-clonic grand mal seizures). partial (focal) epilepsy either alone or as adjuvant therapy.

Epilim EC New Zealand - English - Medsafe (Medicines Safety Authority)

epilim ec

pharmacy retailing (nz) ltd t/a healthcare logistics - sodium valproate 500mg; sodium valproate 500mg; sodium valproate 500mg - modified release tablet - 500 mg - active: sodium valproate 500mg excipient: calcium silicate citric acid diethyl phthalate hypromellose macrogol 6000 magnesium stearate opaspray polyvinylacetate phthalate povidone purified talc stearic acid active: sodium valproate 500mg excipient: calcium silicate citric acid diethyl phthalate hypromellose macrogol 6000 magnesium stearate opaspray polyvinylacetate phthalate povidone purified talc stearic acid active: sodium valproate 500mg excipient: calcium silicate magnesium stearate povidone purified talc violet enteric coat excipient blend violet sub-coat excipient blend - epilepsy: primary generalised epilepsy (petit mal absences, various forms of myoclonic epilepsy and tonic-clonic grand mal seizures). partial (focal) epilepsy either alone or as adjuvant therapy.

Pediamox 100 mg/ mL Powder For Suspension (Oral Drops) Philippines - English - FDA (Food And Drug Administration)

pediamox 100 mg/ ml powder for suspension (oral drops)

unilab, inc. - amoxicillin (as trihydrate) - powder for suspension (oral drops) - 100 mg/ ml

Pediamox 250 mg/5 mL Powder For Suspension Philippines - English - FDA (Food And Drug Administration)

pediamox 250 mg/5 ml powder for suspension

unilab, inc. - amoxicillin (as trihydrate) - powder for suspension - 250 mg/5 ml

DIAMOX Tablets 250 Milligram Ireland - English - HPRA (Health Products Regulatory Authority)

diamox tablets 250 milligram

t. p. whelehan son & co. limited - acetazolamide parenterol hydrochloride - tablets - 250 milligram

DIAMOX PARENTERAL Ireland - English - HPRA (Health Products Regulatory Authority)

diamox parenteral

t. p. whelehan son & co. limited - acetazolamide parenterol hydrochloride -

DIAMOX SUSTETS Ireland - English - HPRA (Health Products Regulatory Authority)

diamox sustets

cyanamid of great britain - capsule - 500 milligram

DIAMOX SUSTETS Ireland - English - HPRA (Health Products Regulatory Authority)

diamox sustets

t. p. whelehan son & co. limited - acetazolamide parenterol hydrochloride -

DIAMOX 10 TAB India - English - Central Drugs Standard Control Organization

diamox 10 tab

wyeth - acetazolamide - tab - 250mg - 10

Diamox New Zealand - English - Medsafe (Medicines Safety Authority)

diamox

wyeth (nz) ltd - acetazolamide sodium 500mg;   - powder for injection - 500 mg - active: acetazolamide sodium 500mg