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2013.8-FDA指南:ANDA:原料药和制剂稳定性试验问答(中英文)

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201308 FDA指南:ANDA:原料药和制剂稳定性试验问答(中英文)

Guidance for Industry 行业指南

ANDAs: Stability Testing of Drug Substances and Products

Questions and Answers

ANDA:原料药和制剂稳定性试验问答

DRAFT GUIDANCE

指南草案

This guidance document is being distributed for comment purposes only. 本指南文件发布仅供讨论。

Comments and suggestions regarding this draft document should be submitted within 60 days of publication in the Federal Register of the notice announcing the availability of the draft guidance. Submit electronic comments

to http://www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. All comments should be identified with the docket number listed in the notice of availability that publishes in the Federal Register. For questions regarding this draft document contact (CDER) Radhika Rajagopalan 240-276-8546.

U.S. Department of Health and Human Services

Food and Drug Administration

Center for Drug Evaluation and Research (CDER)

August 2013 Generics

Guidance for Industry

ANDAs: Stability Testing of Drug Substances and Products

Questions and Answers ANDA:原料药和制剂稳定性试验问答

Additional copies are available from:

Office of Communications

Division of Drug Information, WO51, Room 2201 Center for Drug Evaluation and Research

Food and Drug Administration

10903 New Hampshire Ave., Silver Spring, MD 20993

Phone: 301-796-3400; Fax: 301-847-8714

druginfo@fda.hhs.gov

http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm

U.S. Department of Health and Human Services

Food and Drug Administration

Center for Drug Evaluation and Research (CDER)

August 2013

Generics Contains Nonbinding Recommendations Draft — Not for Implementation

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