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

nebivolol lupin 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.

Nebivolol Accord 5 mg tablets Ireland - English - HPRA (Health Products Regulatory Authority)

nebivolol accord 5 mg tablets

accord healthcare ireland ltd. - nebivolol hydrochloride - tablet - nebivolol

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

nebivolol sandoz 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.

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

nebivolol sandoz 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.

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

nebivolol sandoz 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.

Nebivolol/HCT EG 5 mg - 12.5 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

nebivolol/hct eg 5 mg - 12.5 mg film-coat. tabl.

eg sa-nv - nebivolol hydrochloride 5,45 mg - eq. nebivolol 5 mg; hydrochlorothiazide 12,5 mg - film-coated tablet - 5 mg - 12,5 mg - nebivolol hydrochloride 5.45 mg; hydrochlorothiazide 12.5 mg - nebivolol and thiazides

Nebivolol/HCT EG 5 mg - 25 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

nebivolol/hct eg 5 mg - 25 mg film-coat. tabl.

eg sa-nv - nebivolol hydrochloride 5,45 mg - eq. nebivolol 5 mg; hydrochlorothiazide 25 mg - film-coated tablet - 5 mg - 25 mg - nebivolol hydrochloride 5.45 mg; hydrochlorothiazide 25 mg - nebivolol and thiazides