NEPITEN nebivolol (as hydrochloride) 10 mg immediate release tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

nepiten nebivolol (as hydrochloride) 10 mg immediate release tablet blister pack

southern cross pharma pty ltd - nebivolol hydrochloride, quantity: 10.9 mg (equivalent: nebivolol, qty 10 mg) - tablet - excipient ingredients: lactose monohydrate; maize starch; croscarmellose sodium; hypromellose; polysorbate 80; microcrystalline cellulose; silicon dioxide; magnesium stearate - nebivolol is indicated: - to treat essential hypertension; - to treat stable chronic heart failure as an adjunct to standard therapies in patients 70 years or older.

NEPITEN nebivolol (as hydrochloride) 5 mg immediate release tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

nepiten nebivolol (as hydrochloride) 5 mg immediate release tablet blister pack

southern cross pharma pty ltd - nebivolol hydrochloride, quantity: 5.45 mg (equivalent: nebivolol, qty 5 mg) - tablet - excipient ingredients: lactose monohydrate; maize starch; croscarmellose sodium; hypromellose; polysorbate 80; microcrystalline cellulose; silicon dioxide; magnesium stearate - nebivolol is indicated: - to treat essential hypertension; - to treat stable chronic heart failure as an adjunct to standard therapies in patients 70 years or older.

NEPITEN nebivolol (as hydrochloride) 1.25 mg immediate release tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

nepiten nebivolol (as hydrochloride) 1.25 mg immediate release tablet blister pack

southern cross pharma pty ltd - nebivolol hydrochloride, quantity: 1.363 mg (equivalent: nebivolol, qty 1.25 mg) - tablet - excipient ingredients: lactose monohydrate; maize starch; croscarmellose sodium; hypromellose; polysorbate 80; microcrystalline cellulose; silicon dioxide; magnesium stearate - nebivolol is indicated: - to treat essential hypertension; - to treat stable chronic heart failure as an adjunct to standard therapies in patients 70 years or older.

Nebilet Plus 5 mg / 12.5 mg film-coated tablets Malta - English - Medicines Authority

nebilet plus 5 mg / 12.5 mg film-coated tablets

menarini international operations luxembourg s.a 1 avenue de la gare, l-1611, luxembourg - hydrochlorothiazide, nebivolol hydrochloride - film-coated tablet - hydrochlorothiazide 12.5 mg nebivolol hydrochloride 5 mg - beta blocking agents

Nebivolol Teva 5 mg Tablets Ireland - English - HPRA (Health Products Regulatory Authority)

nebivolol teva 5 mg tablets

teva pharma b.v. - nebivolol - tablet - 5 milligram(s) - beta blocking agents, selective; nebivolol

Nebivolol 10mg tablets Ireland - English - HPRA (Health Products Regulatory Authority)

nebivolol 10mg tablets

glenmark arzneimittel gmbh - nebivolol - tablet - 10 milligram(s) - beta blocking agents, selective; nebivolol

Nebivolol 10mg tablets Ireland - English - HPRA (Health Products Regulatory Authority)

nebivolol 10mg tablets

glenmark pharmaceuticals europe limited - nebivolol - tablet - 10 milligram(s) - beta blocking agents, selective; nebivolol

Nebivolol STELLA Tablet 5mg Malaysia - English - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

nebivolol stella tablet 5mg

stadpharm sdn. bhd. - nebivolol hydrochloride -

Nebivolol 2.5mg tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

nebivolol 2.5mg tablets

a a h pharmaceuticals ltd - nebivolol hydrochloride - oral tablet - 2.5mg

Nebivolol 2.5mg tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

nebivolol 2.5mg tablets

alliance healthcare (distribution) ltd - nebivolol hydrochloride - oral tablet - 2.5mg