{"abstract":"The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register of June 25, 2021. The document announced the withdrawal of approval of 36 abbreviated new drug applications (ANDAs) from multiple applicants as of July 26, 2021. The document indicated that FDA was withdrawing approval of the following ANDA, after receiving a withdrawal request from Yung Shin Pharmaceutical Ind. Co. Ltd., authorized U.S. agent, Carlsbad Technology, Inc./Simon Law, 5922 Farnsworth Ct., Suite 101, Carlsbad, CA 92008: ANDA 065152, Cephalexin Capsules, Equivalent to (EQ) 250 milligrams (mg) base and EQ 500 mg base. Before FDA withdrew the approval of this ANDA, Yung Shin Pharmaceutical Ind. Co. Ltd. informed FDA that it did not want the approval of the ANDA withdrawn. Because Yung Shin Pharmaceutical Ind. Co. Ltd. timely requested that approval of this ANDA not be withdrawn, the approval of ANDA 065152 is still in effect.","action":"Notice; correction.","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"body_html_url":"https://www.federalregister.gov/documents/full_text/html/2021/10/01/2021-21371.html","cfr_references":[],"citation":"86 FR 54450","comment_url":null,"comments_close_on":null,"correction_of":null,"corrections":[],"dates":null,"disposition_notes":null,"docket_ids":["Docket No. FDA-2021-N-0492"],"dockets":[],"document_number":"2021-21371","effective_on":null,"end_page":54450,"executive_order_notes":null,"executive_order_number":null,"explanation":null,"full_text_xml_url":"https://www.federalregister.gov/documents/full_text/xml/2021/10/01/2021-21371.xml","html_url":"https://www.federalregister.gov/documents/2021/10/01/2021-21371/watson-laboratories-inc-et-al-withdrawal-of-approval-of-36-abbreviated-new-drug-applications","images":{},"images_metadata":{},"json_url":"https://www.federalregister.gov/api/v1/documents/2021-21371?publication_date=2021-10-01","mods_url":"https://www.govinfo.gov/metadata/granule/FR-2021-10-01/2021-21371/mods.xml","not_received_for_publication":null,"page_length":1,"page_views":{"count":166,"last_updated":"2026-04-04 14:15:05 -0400"},"pdf_url":"https://www.govinfo.gov/content/pkg/FR-2021-10-01/pdf/2021-21371.pdf","presidential_document_number":null,"proclamation_number":null,"public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2021-21371.pdf?1633005929","publication_date":"2021-10-01","raw_text_url":"https://www.federalregister.gov/documents/full_text/text/2021/10/01/2021-21371.txt","regulation_id_number_info":{},"regulation_id_numbers":[],"regulations_dot_gov_info":{"supporting_documents":[],"comments_count":0,"agency_id":"FDA","comments_url":"https://www.regulations.gov/docketBrowser?rpp=50&so=DESC&sb=postedDate&po=0&dct=PS&D=FDA-2021-N-0492","supporting_documents_count":0,"docket_id":"FDA-2021-N-0492","document_id":"FDA-2021-N-0492-0002","regulation_id_number":null,"title":"Watson Laboratories, Inc., et al.; Withdrawal of Approval of 36 Abbreviated New Drug Applications","checked_regulationsdotgov_at":"2021-10-05T03:30:10Z"},"regulations_dot_gov_url":null,"significant":null,"signing_date":null,"start_page":54450,"subtype":null,"title":"Watson Laboratories, Inc., et al.; Withdrawal of Approval of 36 Abbreviated New Drug Applications; Correction","toc_doc":"Watson Laboratories, Inc., et al.; Withdrawal of Approval; Correction","toc_subject":"New Drug Applications:\n","topics":[],"type":"Notice","volume":86}