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Products
Finished Dosage Forms
Tablets
Immediate-Release Tablets

ポラキス錠1

チェ

チェプラファーム株式会社

Marketing Authorization Holder · Finished Dosage FormsJapan

Basic Information

Category

Subcategory & Sub-subcategory

/

Trade Type

Sell

Product Name

ポラキス錠1

Details

• •

Substance

Registered Market

Specifications

Dosage Form: Tablet

Documents

Drug Marketing Authorization Number

Document No.: 20400AMZ00551

Issue Date: Aug 1, 1992

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Finished Dosage Forms

Immediate-Release Tablets

分1錠中日局オキシブチニン塩酸塩 1 mg

日局オキシブチニン塩酸塩 2 mg

日局オキシブチニン塩酸塩 3 mg

Oxybutynin Hydrochloride

ポラキス錠1 | Pharmacountry