[Federal Register: December 4, 2000 (Volume 65, Number 233)]
[Notices]
[Page 75717-75718]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr04de00-91]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 00N-1639]
SangStat Medical Corp.; Withdrawal of Approval of an Abbreviated
New Drug Application; Cyclosporine
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is withdrawing approval
of an abbreviated new drug application (ANDA) held by SangStat Medical
Corp., 6300 Dumbarton Circle, Fremont, CA 94555 (Sangstat). The ANDA is
for SangCya Oral Solution (Cyclosporine Oral Solution, USP) Modified,
which was the subject of a class II recall announced on July 10, 2000.
SangStat has agreed in writing to
[[Page 75718]]
permit FDA to withdraw approval of the application and has waived its
opportunity for a hearing.
EFFECTIVE DATES: January 3, 2001.
FOR FURTHER INFORMATION CONTACT: David T. Read, Center for Drug
Evaluation and Research (HFD-7), Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857, 301-594-2041.
SUPPLEMENTARY INFORMATION: On July 10, 2000, SangCya Oral Solution
(Cyclosporine Oral Solution, USP) Modified, 100 milligrams per
milliliter, was the subject of a class II recall under 21 CFR part 7
(Ref. 1). The recall of the drug product, marketed under ANDA 64-195,
arose from data recently submitted by SangStat to the agency regarding
the bioavailability of the product in healthy subjects when
administered with apple juice. Following the recall, SangStat notified
the agency in writing on July 21, 2000, that the company had decided to
permanently withdraw the product from the market. On August 4, 2000,
SangStat requested in writing that the agency withdraw approval of ANDA
64-195. Subsequently, SangStat provided the agency with a full and
complete waiver of the company's right to a hearing under section
505(e) of the Federal Food, Drug, and Cosmetic Act (the act) (21 U.S.C.
355(e)) to allow the agency to complete the withdrawal of approval
under 21 CFR 314.150(d).
Therefore, under section 505(e) of the act and under authority
delegated to the Director, Center for Drug Evaluation and Research (21
CFR 5.82), approval of ANDA 64-195, and all amendments and supplements
thereto, is hereby withdrawn, effective January 3, 2001. The effective
date of the withdrawal of approval is intended to allow patients the
opportunity to complete their transition to another cyclosporine drug
product (see Ref. 1). Thereafter, distribution of the product in
interstate commerce without an approved application is illegal and
subject to regulatory action. Also, on the basis of the circumstances
described above that led to the recall of the product and its
subsequent removal from the market, the agency will remove the product
from the agency's list of drug products with effective approvals,
published under the title ``Approved Drug Products with Therapeutic
Equivalence Evaluations.'' This document serves as notice of the
removal of the product covered by ANDA 64-195, SangCya Oral Solution,
from the list of approved drug products.
Reference
The following reference has been placed on display in the Dockets
Management Branch (HFA-305), Food and Drug Administration, 5630 Fishers
Lane, rm. 1061, Rockville, MD 20852. The document may be seen by
interested persons between 9 a.m. and 4 p.m., Monday through Friday.
The document is available on the Internet at: http:www//fda.gov/bbs/
topics/ANSWERS/ANS01025.html.
1. FDA Talk Paper dated July 10, 2000.
Dated: November 21, 2000.
Janet Woodcock,
Director, Center for Drug Evaluation and Research.
[FR Doc. 00-30773 Filed 12-1-00; 8:45 am]
BILLING CODE: 3510-22-S