PREGABALIN LAPL pregabalin 20 mg/mL oral solution bottle

국가: 오스트레일리아

언어: 영어

출처: Department of Health (Therapeutic Goods Administration)

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공공 평가 보고서 공공 평가 보고서 (PAR)
26-11-2017

유효 성분:

pregabalin, Quantity: 20 mg/mL

제공처:

Lupin Australia Pty Limited

INN (International Name):

Pregabalin

약제 형태:

Oral Liquid, solution

구성:

Excipient Ingredients: sucralose; monobasic sodium phosphate monohydrate; purified water; dibasic sodium phosphate; propyl hydroxybenzoate; methyl hydroxybenzoate; Flavour

관리 경로:

Oral

패키지 단위:

1

처방전 유형:

(S4) Prescription Only Medicine

치료 징후:

Pregabalin LAPL is indicated for the treatment of neuropathic pain in adults. Pregabalin LAPL is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

제품 요약:

Visual Identification: A clear colorless liquid with characteristic banana odor.; Container Type: Bottle; Container Material: HDPE; Container Life Time: 6 Months; Container Temperature: Store below 25 degrees Celsius; Container Closure: Child resistant closure

승인 상태:

Licence status A

승인 날짜:

2014-12-05