Tanzania - English - Tanzania Medicinces & Medical Devices Authority

unichem laboratories limited, india - memantine - film coated tablet - 10

Tanzania - English - Tanzania Medicinces & Medical Devices Authority

unichem laboratories limited, india - memantine - film coated tablet - 10

Australia - English - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - propantheline bromide, quantity: 15 mg - tablet, film coated - excipient ingredients: maize starch; lactose monohydrate; magnesium stearate; purified talc; titanium dioxide; sunset yellow fcf aluminium lake; iron oxide yellow; polyvinyl alcohol; macrogol 3350; lecithin; indigo carmine aluminium lake - this product accepted for registration as 'currently supplied' at the time of commencement of the act. indications were approved as specified in the letter of 7 april 1993 from dr l. hunt are as follows: as an adjunctive therapy in the treatment of peptic ulcer (gastric and duodenal), neurogenic bladder, urinary incontinence in patients with detrusor hyperactivity and hyperhidrosis.

Australia - English - Department of Health (Therapeutic Goods Administration)

sun pharma anz pty ltd - memantine hydrochloride, quantity: 10 mg - tablet, film coated - excipient ingredients: croscarmellose sodium; colloidal anhydrous silica; magnesium stearate; microcrystalline cellulose; purified talc; titanium dioxide; hypromellose; macrogol 400 - treatment of the symptoms of moderately severe to severe alzheimer's disease

Australia - English - Department of Health (Therapeutic Goods Administration)

sun pharma anz pty ltd - memantine hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: magnesium stearate; purified talc; microcrystalline cellulose; colloidal anhydrous silica; croscarmellose sodium; titanium dioxide; hypromellose; iron oxide yellow; iron oxide red; macrogol 400 - treatment of the symptoms of moderately severe to severe alzheimer's disease

Australia - English - Department of Health (Therapeutic Goods Administration)

sun pharma anz pty ltd - memantine hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: purified talc; microcrystalline cellulose; croscarmellose sodium; magnesium stearate; colloidal anhydrous silica; titanium dioxide; hypromellose; iron oxide yellow; iron oxide red; macrogol 400 - treatment of the symptoms of moderately severe to severe alzheimer's disease

Australia - English - Department of Health (Therapeutic Goods Administration)

sun pharma anz pty ltd - memantine hydrochloride, quantity: 10 mg - tablet, film coated - excipient ingredients: magnesium stearate; purified talc; croscarmellose sodium; colloidal anhydrous silica; microcrystalline cellulose; titanium dioxide; hypromellose; macrogol 400 - treatment of the symptoms of moderately severe to severe alzheimer's disease

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

apotex europe b.v. - memantine hydrochloride 10 mg - film-coated tablet - 10 mg - memantine hydrochloride 10 mg - memantine

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

apotex europe b.v. - memantine hydrochloride 20 mg - film-coated tablet - 20 mg - memantine hydrochloride 20 mg - memantine

Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

eg sa-nv - memantine hydrochloride 10 mg - eq. memantine 8,31 mg - film-coated tablet - 10 mg - memantine hydrochloride 10 mg - memantine