Determinations that Drugs were Not Withdrawn from Sale for Reasons of Safety or Effectiveness:

Federal Register Volume 76, Number 168 (Tuesday, August 30, 2011)

Notices

Pages 53907-53908

From the Federal Register Online via the Government Printing Office [www.gpo.gov]

FR Doc No: 2011-22145

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

Docket No. FDA-2011-P-0460

Determination That TALWIN COMPOUND (Aspirin; Pentazocine

Hydrochloride) Tablets, 325 Milligrams; Equivalent to 12.5 Milligram

Base, Were Not Withdrawn From Sale for Reasons of Safety or

Effectiveness

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

SUMMARY: The Food and Drug Administration (FDA) has determined that

TALWIN COMPOUND (aspirin; pentazocine hydrochloride (HCl)) tablets, 325 milligrams (mg); equivalent to (EQ) 12.5 mg base, were not withdrawn from sale for reasons of safety or effectiveness. This determination will allow FDA to approve abbreviated new drug applications (ANDAs) for aspirin; pentazocine HCl tablets, 325 mg; EQ 12.5 mg base, if all other legal and regulatory requirements are met.

FOR FURTHER INFORMATION CONTACT: Nam Kim, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave.,

Bldg. 51, rm. 6320, Silver Spring, MD 20993-0002, 301-796-3601.

SUPPLEMENTARY INFORMATION: In 1984, Congress enacted the Drug Price

Competition and Patent Term Restoration Act of 1984 (Pub. L. 98-417)

(the 1984 amendments), which authorized the approval of duplicate versions of drug products under an ANDA procedure. ANDA applicants must, with certain exceptions, show that the drug for which they are seeking approval contains the same active ingredient in the same strength and dosage form as the ``listed drug,'' which is a version of the drug that was previously approved. ANDA applicants do not have to repeat the extensive clinical testing otherwise necessary to gain approval of a new drug application (NDA). The only clinical data required in an ANDA are data to show that the drug that is the subject of the ANDA is bioequivalent to the listed drug.

The 1984 amendments include what is now section 505(j)(7) of the

Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355(j)(7)), which requires FDA to publish a list of all approved drugs. FDA publishes this list as part of the ``Approved Drug Products with Therapeutic

Equivalence Evaluations,'' which is known generally as the ``Orange

Book.'' Under FDA regulations, drugs are removed from the list if the

Agency withdraws or suspends approval of the drug's NDA or ANDA for reasons of safety or effectiveness or if FDA determines that the listed drug was withdrawn from sale for reasons of safety or effectiveness (21

CFR 314.162).

A person may petition the Agency to determine, or the Agency may determine on its own initiative, whether a listed drug was withdrawn from sale for reasons of safety or effectiveness. This determination may be made at any time after the drug has been withdrawn from sale, but must be made prior to approving an ANDA that refers to the listed drug (Sec. 314.161 (21 CFR 314.161)). FDA may not approve an ANDA that does not refer to a listed drug.

TALWIN COMPOUND (aspirin; pentazocine HCl) tablets, 325 mg; EQ 12.5 mg base, are the subject of NDA 016891, held by Sanofi-aventis U.S., and initially approved on November 12, 1975. TALWIN COMPOUND tablets are indicated for the relief of moderate pain.

TALWIN COMPOUND (aspirin; pentazocine HCl) tablets, 325 mg; EQ 12.5 mg base, are currently listed in the

Page 53908

``Discontinued Drug Product List'' section of the Orange Book.

Lachman Consultant Services, Inc., submitted a citizen petition dated June 7, 2011 (Docket No. FDA-2011-P-0460), under 21 CFR 10.30, requesting that the Agency determine whether TALWIN COMPOUND (aspirin; pentazocine HCl) tablets, 325 mg; EQ 12.5 mg base, have been voluntarily withdrawn or withheld from sale for reasons of safety or effectiveness.

After considering the citizen petition and reviewing Agency records and based on the information we have at this time, FDA has determined under Sec. 314.161 that TALWIN COMPOUND (aspirin; pentazocine HCl) tablets, 325 mg; EQ 12.5 mg base, were not withdrawn for reasons of safety or effectiveness. The petitioner has identified no data or other information suggesting that TALWIN COMPOUND (aspirin; pentazocine HCl) tablets, 325 mg; EQ 12.5 mg base, were withdrawn for reasons of safety or effectiveness. We have carefully reviewed our files for records concerning the withdrawal of TALWIN COMPOUND (aspirin; pentazocine HCl) tablets, 325 mg; EQ 12.5 mg base, from sale. We have also independently evaluated relevant literature and data for possible postmarketing adverse events. We have found no information that would indicate that this product was withdrawn from sale for reasons of safety or effectiveness.

Accordingly, the Agency will continue to list TALWIN COMPOUND

(aspirin; pentazocine HCl) tablets, 325 mg; EQ 12.5 mg base, in the

``Discontinued Drug Product List'' section of the Orange Book. The

``Discontinued Drug Product List'' delineates, among other items, drug products that have been discontinued from marketing for reasons other than safety or effectiveness. ANDAs that refer to TALWIN COMPOUND

(aspirin; pentazocine HCl) tablets, 325 mg; EQ 12.5 mg base, may be approved by the Agency as long as they meet all other legal and regulatory requirements for the approval of ANDAs. If FDA determines that labeling for this drug product should be revised to meet current standards, the Agency will advise ANDA applicants to submit such labeling.

Dated: August 25, 2011.

Leslie Kux,

Acting Assistant Commissioner for Policy.

FR Doc. 2011-22145 Filed 8-29-11; 8:45 am

BILLING CODE 4160-01-P