Search for FDA-Approved Drugs - Drugs | 合法醫療器材資訊網

References Click to view CHORIONIC GONADOTROPIN (GONADOTROPIN, CHORIONIC) (www.accessdata.fda.gov) Click to view ANGELIQ (DROSPIRENONE; ESTRADIOL) (www.accessdata.fda.gov) Click to view ANGELIQ (DROSPIRENONE; ESTRADIOL) (www.accessdata.fda.gov) Click to view MONTELUKAST SODIUM (MONTELUKAST SODIUM) (www.accessdata.fda.gov) Click to view MONTELUKAST SODIUM (MONTELUKAST SODIUM) (www.accessdata.fda.gov) Click to view VELTASSA (PATIROMER SORBITEX CALCIUM) (www.accessdata.fda.gov) Click to view SUCCINYLCHOLINE CHLORIDE (SUCCINYLCHOLINE CHLORIDE) (www.accessdata.fda.gov) Click to view ARIPIPRAZOLE (ARIPIPRAZOLE) (www.accessdata.fda.gov) Click to view TRA...

How do I find out if a drug is approved? Is there a Web site I ... | 合法醫療器材資訊網

Approvals of FDA | 合法醫療器材資訊網

2018年3月29日 — Approval information by product type. ... or diagnosing disease (such as thermometers, artificial hearts, and home pregnancy test kits). Read More

Search Databases | 合法醫療器材資訊網

2021年2月1日 — Animal Drugs @ FDA is an online database of FDA-approved animal drugs. ... Disclosure of the compliance status of firms helps to provide the ... Read More

Drug Approvals and Databases | 合法醫療器材資訊網

2020年6月18日 — Additional topics include: approved REMS, drug shortages, and the Orange ... Inactive Ingredient Search for Approved Drug Products Search Read More

Search Registration and Listing | 合法醫療器材資訊網

2017年12月23日 — Releasable establishment registration and listing information under the Freedom of Information Act is available by searching the Establishment ... Read More

Device Approvals | 合法醫療器材資訊網

2018年3月26日 — Search the PMA Database. Regulation also provides for the submission of a humanitarian device exemption (HDE) application. Read More

Drugs@FDA | 合法醫療器材資訊網

Drugs@FDA: FDA-Approved Drugs · Search by Drug Name, Active Ingredient, or Application Number* · Browse by Drug Name. Read More

Search for FDA-Approved Drugs - Drugs | 合法醫療器材資訊網

Recent New and Generic Drug Approvals - Drugs | 合法醫療器材資訊網

For comprehensive approval reports, please use the monthly All Approvals report on Drugs@FDA. 7 Day Report; 14 Day Report. July 14, 2021. Drug Name and Read More

510(k) Premarket Notification | 合法醫療器材資訊網

... that is, substantially equivalent, to a legally marketed device (section 513(i)(1)(A) FD&C Act) that is not subject to premarket approval. Read More

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