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

eraldin

astrazeneca limited - practolol 100mg - tablet - 100 mg - active: practolol 100mg

ERALDIN Withdrawn Form Ireland - English - HPRA (Health Products Regulatory Authority)

eraldin withdrawn form

zeneca limited - practolol - withdrawn form

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

nebol 5 mg tablets

rowex ltd - nebivolol hydrochloride - tablet - 5 milligram(s) - beta blocking agents, selective; nebivolol

NEBILET TABLET 5 mg Singapore - English - HSA (Health Sciences Authority)

nebilet tablet 5 mg

a. menarini singapore pte. ltd. - nebivolol hydrochloride 5.45mg (equivalent to nebivolol) - tablet - 5mg - nebivolol hydrochloride 5.45mg (equivalent to nebivolol) 5mg

Nebivolol Actavis 5mg Tablets 5mg Malta - English - Medicines Authority

nebivolol actavis 5mg tablets 5mg

actavis group ptc ehf revkjavikurvegi 76-78, 220 hafnarfjordur, iceland - nebivolol hydrochloride - tablet - nebivolol hydrochloride 5 mg - beta blocking agents

Nebivolol 5mg tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

nebivolol 5mg tablets

sandoz ltd - nebivolol hydrochloride - oral tablet - 5mg

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

nebilet

a menarini australia pty ltd - nebivolol hydrochloride -

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.