2014-09898. Actavis Totowa LLC, et al.; Withdrawal of Approval of Abbreviated New Drug Applications for Prescription Pain Medications Containing More Than 325 Milligrams of Acetaminophen; Correction
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AGENCY:
Food and Drug Administration, HHS.
ACTION:
Notice; correction.
SUMMARY:
The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register of March 27, 2014 (79 FR 17163). The document withdrew approval of 108 abbreviated new drug applications (ANDAs) for prescription pain medications containing more than 325 milligrams (mg) of acetaminophen per dosage unit from multiple applicants, effective March 27, 2014. The document failed to withdraw approval of ANDAs 040825, 040822, and 040824, held by Ranbaxy Laboratories Inc. and Ranbaxy Inc., 600 College Rd. East, Princeton, NJ 08540, and ANDA 040182, held by Pharmaceutical Associates, Inc., 201 Delaware St., Greenville, SC 29605. The holders of these applications have voluntarily requested that approval of these applications be withdrawn and have waived their opportunity for a hearing. FDA confirms the withdrawal of approval of ANDAs 040825, 040824, 040822, and 040182.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Rachel Turow, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 51, Rm. 6236, Silver Spring, MD 20993-0002, 301-796-5094.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
In FR Doc. 2014-06801, appearing on page 17163, in the Federal Register of Thursday, March 27, 2014, the following correction is made:
On page 17166, in table 1, the following entries are added in alphabetical order by Applicant:
Start SignatureApplication No. Drug product(s) Applicant or holder ANDA 040182 Acetaminophen and Hydrocodone Bitartrate Oral Solution, 7.5 mg/500 mg/15 milliters (mL), available in 473 mL, 118 mL, 15 mL, and 10 mL Pharmaceutical Associates, Inc., 201 Delaware St., Greenville, SC 29605. ANDA 040825 Acetaminophen and Hydrocodone Bitartrate Tablets, 500 mg/5 mg Ranbaxy Laboratories Inc., 600 College Rd. East, Princeton, NJ 08540. ANDA 040822 Acetaminophen and Hydrocodone Bitartrate Tablets, 750 mg/7.5 mg Do. ANDA 040824 Acetaminophen and Hydrocodone Bitartrate Tablets, 500 mg/10 mg Ranbaxy Inc., 600 College Rd. East, Princeton, NJ 08540. Dated: April 24, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014-09898 Filed 4-30-14; 8:45 am]
BILLING CODE 4160-01-P
Document Information
- Published:
- 05/01/2014
- Department:
- Food and Drug Administration
- Entry Type:
- Notice
- Action:
- Notice; correction.
- Document Number:
- 2014-09898
- Pages:
- 24734-24734 (1 pages)
- Docket Numbers:
- Docket No. FDA-2011-N-0021
- PDF File:
- 2014-09898.pdf
- Supporting Documents:
- » Reference 1 - FDA Center for Drug Evaluation and Research, Acetaminophen Overdose and Liver Injury--Background and Options for Reducing Injury, Available on FDA's Web site at http;//www.fda.gov/AdvisoryCommittee/CommitteesMeetingMaterials/Drugs/DrugsSafet