LURACOR lurasidone hydrochloride 40 mg film-coated tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

luracor lurasidone hydrochloride 40 mg film-coated tablet bottle

pharmacor pty ltd - lurasidone hydrochloride, quantity: 40 mg - tablet, film coated - excipient ingredients: citric acid; lactose monohydrate; magnesium stearate; povidone; croscarmellose sodium; mannitol; pregelatinised maize starch; titanium dioxide; hypromellose; macrogol 400 - lurasidone hydrochloride film-coated tablets are indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

PHARMACOR LURASIDONE lurasidone hydrochloride 40 mg film-coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

pharmacor lurasidone lurasidone hydrochloride 40 mg film-coated tablet blister pack

pharmacor pty ltd - lurasidone hydrochloride, quantity: 40 mg - tablet, film coated - excipient ingredients: magnesium stearate; povidone; lactose monohydrate; citric acid; pregelatinised maize starch; croscarmellose sodium; titanium dioxide; hypromellose; macrogol 400 - lurasidone hydrochloride film-coated tablets are indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

PHARMACOR LURASIDONE lurasidone hydrochloride 40 mg film-coated tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

pharmacor lurasidone lurasidone hydrochloride 40 mg film-coated tablet bottle

pharmacor pty ltd - lurasidone hydrochloride, quantity: 40 mg - tablet, film coated - excipient ingredients: lactose monohydrate; pregelatinised maize starch; mannitol; citric acid; croscarmellose sodium; povidone; magnesium stearate; titanium dioxide; hypromellose; macrogol 400 - lurasidone hydrochloride film-coated tablets are indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

LURACOR lurasidone hydrochloride 20 mg film-coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

luracor lurasidone hydrochloride 20 mg film-coated tablet blister pack

pharmacor pty ltd - lurasidone hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: citric acid; croscarmellose sodium; lactose monohydrate; povidone; mannitol; magnesium stearate; pregelatinised maize starch; titanium dioxide; hypromellose; macrogol 400 - lurasidone hydrochloride film-coated tablets are indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

LURACOR lurasidone hydrochloride 20 mg film-coated tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

luracor lurasidone hydrochloride 20 mg film-coated tablet bottle

pharmacor pty ltd - lurasidone hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: magnesium stearate; citric acid; povidone; croscarmellose sodium; lactose monohydrate; pregelatinised maize starch; mannitol; titanium dioxide; hypromellose; macrogol 400 - lurasidone hydrochloride film-coated tablets are indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

PHARMACOR LURASIDONE lurasidone hydrochloride 20 mg film-coated tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

pharmacor lurasidone lurasidone hydrochloride 20 mg film-coated tablet blister pack

pharmacor pty ltd - lurasidone hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: croscarmellose sodium; citric acid; lactose monohydrate; mannitol; magnesium stearate; povidone; pregelatinised maize starch; titanium dioxide; hypromellose; macrogol 400 - lurasidone hydrochloride film-coated tablets are indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

PHARMACOR LURASIDONE lurasidone hydrochloride 20 mg film-coated tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

pharmacor lurasidone lurasidone hydrochloride 20 mg film-coated tablet bottle

pharmacor pty ltd - lurasidone hydrochloride, quantity: 20 mg - tablet, film coated - excipient ingredients: povidone; mannitol; pregelatinised maize starch; lactose monohydrate; citric acid; magnesium stearate; croscarmellose sodium; titanium dioxide; hypromellose; macrogol 400 - lurasidone hydrochloride film-coated tablets are indicated for the treatment of schizophrenia in adults and adolescents (aged 13 to 17 years).

Ilium Thiopentone New Zealand - English - Ministry for Primary Industries

ilium thiopentone

troy laboratories pty limited - thiopental sodium - thiopental sodium 1,000 g/kg - anaesthetic

Thiopental Injection BP 500 mg Powder For Solution For Injection Kenya - English - Pharmacy and Poisons Board

thiopental injection bp 500 mg powder for solution for injection

rotexmedica gmbh arzneimittelwerk bunsenstrasse 4, 22946 trittau, germany - thiopental sodium - powder for solution for injection - 1 vial contains 500 mg thiopental sodium - general anesthetics: plain barbiturates

Pentothal thiopental sodium 500 mg powder for injection vial Australia - English - Department of Health (Therapeutic Goods Administration)

pentothal thiopental sodium 500 mg powder for injection vial

link medical products pty ltd t/a link pharmaceuticals - thiopental sodium, quantity: 0.5 g - injection, powder for - excipient ingredients: - indications as at 08 dec 1993 : pentothal may be used : 1. as the sole anaesthetic agent for brief surgical procedures; 2. for the induction of anaesthesia prior to the administration of other anaesthetic agents; 3. for the short-term control of condvulsive states; 4. to supplement regional anaesthesia or low potency agents such as nitrous oxide.