1117-0047 Supporting Statement 09.28.2023 DEA Quota FR

1117-0047 Supporting Statement 09.28.2023 DEA Quota FR.docx

Application for Import Quota for Ephedrine, Pseudoephedrine, and Phenylpropanolamine (DEA Form 488)

OMB: 1117-0047

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Application for Import Quota for Ephedrine, Pseudoephedrine, and Phenylpropanolamine – DEA Form 488

OMB Control Number 1117-0047

OMB Expiration Date: 09/30/2025



SUPPORTING STATEMENT FOR

Application for Import Quota for Ephedrine, Pseudoephedrine, and Phenylpropanolamine (DEA Form 488)


The Drug Enforcement Administration (DEA) seeks approval by the Office of Management and Budget (OMB) for an existing collection of information that was previously approved by OMB – OMB Approval #1117-0047, Application for Procurement Quota for Ephedrine, Pseudoephedrine, and Phenylpropanolamine (DEA Form 488).


This information collection request includes changes associated with DEA’s Management of Quotas for Controlled Substances and List I Chemicals rulemaking, RIN 1117-AB49. DEA is formally implementing the use of subcategories to facilitate the issuance of import quotas and provide a more accurate calculation of the assessment of annual needs for the United States. DEA proposes the addition of the following five subcategories for quota: (1) Quota for Commercial Sales; (2) Quota for Transfer; (3) Quota for Product Development; (4) Quota for Replacement; and (5) Quota for Packaging/Repackaging and Labeling/Relabeling. All types of quota can be requested using the same application and format registrants are accustomed to using, in an online form. Importers of list I chemicals will continue to receive import quotas appropriate to their manufacturing and inventory requirements, and DEA will retain greater control over the amount of these listed chemicals produced, thereby reducing the number of inventories at risk of diversion.


  1. JUSTIFICATION


1. The Controlled Substances Act requires the Attorney General to establish aggregate production quota and assessment of annual needs years for each basic class of controlled substance listed in schedules I and II and the list I chemicals ephedrine, pseudoephedrine, and phenylpropanolamine. 21 U.S.C. 826. Pursuant to 21 U.S.C. 952 and 21 CFR 1315.34, any person who desires to import the List I chemicals Ephedrine, Pseudoephedrine, or Phenylpropanolamine during the next calendar year must apply on DEA Form 488 for an import quota for each such List I chemicals. DEA is required to limit the importation of ephedrine, pseudoephedrine, and phenylpropanolamine to the amounts “necessary to provide for medical, scientific, or other legitimate purposes." 21 U.S.C. 952.


2. DEA uses DEA Form 488 to determine the estimated need for ephedrine, pseudoephedrine, and phenylpropanolamine and to establish import quotas for persons importing these List I chemicals. Persons importing ephedrine, pseudoephedrine, and phenylpropanolamine must apply on DEA Form 488 each year for an import quota for each such List I chemical. 21 CFR 1315.34.


3. DEA Form 488 is available to be completed and submitted electronically on the DEA Diversion Control Program website, at https://www.deadiversion.usdoj.gov. Currently, 100% of DEA Form 488 applications are submitted electronically.


4. Controlled substance and listed chemical quotas are unique to DEA. Therefore, there is no duplication of information requested as part of this collection.



5. DEA does not anticipate any additional impact on small businesses or other small entities with the approval of this form. The collection will not have a significant economic impact on small businesses or other small entities within the meaning and intent of the Regulatory Flexibility Act (5 U.S.C. 601–612).


6. If the collection was not conducted or conducted less frequently, DEA would not have sufficient data to set procurement quotas and would be unable to determine the amounts necessary to meet medical, scientific, and other legitimate needs.


7. There are no special circumstances applicable to this information collection.


8. Public comment was solicited in the notice of proposed rulemaking for “Management of Quotas for Controlled Substances and List I Chemicals,” which published in the Federal Register on October 23, 2019 at 84 FR 56712. All comments were addressed in the final rule, published in the Federal Register on August 31, 2023, at 88 FR 60117.


DEA meets regularly with the affected industry to discuss policies, programs, and regulations. These meetings provide an open forum to discuss matters of mutual concern with representatives of those entities from whom the information is obtained.


9. This collection of information does not provide any payment or gift to respondents.


10. Information requested in this collection may be considered confidential business information if marked as such in accordance with 28 CFR 16.8(c) and Exemption 4 of the Freedom of Information Act (FOIA). Submitters who are required to furnish commercial or financial information to the government are protected from the competitive disadvantages that could result from disclosure of such information. The information is protected by DEA through secure storage, limited access, and federal regulatory and DEA procedures. In the event a FOIA request is made to obtain information that has been designated as confidential business information per 28 CFR 16.8(c) and Exemption 4 of FOIA, DEA will give written notice to the submitter to allow an opportunity to object within a reasonable time prior to any disclosure by DEA.



11. This collection of information does not ask any questions of a sensitive nature.



12.



Estimated Annualized Respondent Cost and Hour Burden

Activity

Number of Respondents

Frequency

Total Annual Responses

Time Per Response

Total Annual Burden (Hours)

DEA Form 488

49


126

30 mins

63

Unduplicated Totals

49

N/A

126

30 mins

63 hrs


Percent of responses received electronically: 100%


Hour burden cost:

Estimate hourly wage ($/hour):1

$61.94

Load for benefits (percent of labor rate):2

43.5%

Loaded labor rate ($/hour):3

$88.88

Average burden per response (hour):

0.5

Burden cost per response:

$44.44

Number of annual responses:

126

Total annual burden dollar:

$5,599


13. The annual IC cost burden for this collection is $0.



14. Estimated Annual Labor Cost to Government:


Labor Category4

Number

% of time

Cost5

Section Chief/Supervisory Physical Scientist – GS-1301-15

1

10%

$ 24,481

Analysis of Quota Information (List I chemicals ephedrine, pseudoephedrine, and phenylpropanolamine):

Drug Science Specialists – GS-601-14

1

29%

$ 60,357

Supervisory Physical Scientist - GS-1301-14

1

10%

$ 20,813

Secretary - GS-318-7

1

19%

$ 15,864

Total



$121,516


Total cost to the Federal Government: $121,516.


All costs are recovered from registrants through registration fees, as required by the CSA. 21 U.S.C. 886a.


15. There are no changes in burden for this information collection request. The changes to this collection will formally implement the use of subcategories, and will not change the amount of time needed for respondents to complete responses. The table below summarizes the changes since the last renewal of this information collection.




2022 Approved Burden

New Requested Burden

Difference

Annual responses

3,066

3,066

0

Annual burden hours

1,533

1,533

0

Annual burden dollars

$136,253

$136,253

$0



16. DEA will not publish the results of the information collected.


17. DEA does not object to displaying the expiration date for this collection.


18. DEA is not seeking an exception to the certification statement “Certification for Paperwork Reduction Act Submissions” for this collection of information.


B. COLLECTIONS OF INFORMATON EMPLOYING STATISTICAL METHODS.

This collection does/does not contain statistical data.

1 Hourly median wage, 11-3061 Purchasing Managers for North American Industry Classification System code 325400 – Pharmaceutical and Medicine Manufacturing. Bureau of Labor Statistics, Occupational and Employment and Wages, May 2017, https://www.bls.gov/oes/2017/may/naics4_325400.htm.

2 Average benefits for private industry are 30.3% of total compensation. Bureau of Labor Statistics, Employer Costs for Employee Compensation – September 2018 (ECEC), https://www.bls.gov/news.release/archives/ecec_12142018.pdf. The 30.3% of total compensation equates to 43.5% (30.3% / 69.7%) load on wages and salaries.

3 $61.94 x (1 + 0.435) = $88.88.

4 All government labor costs are rounded to the nearest dollar. Costs are based on the Office of Personnel Management’s 2018 general schedule locality pay tables for the Washington-Baltimore-Arlington area (https://www.opm.gov/policy-data-oversight/pay-leave/salaries-wages/salary-tables/pdf/2018/DCB.pdf) for the grade listed, step 5.

5 Figures are rounded. Government salary figures include 60.26% load for benefits based on the ECEC for State and local government. The ECEC does not include figures for the Federal government.

5


File Typeapplication/vnd.openxmlformats-officedocument.wordprocessingml.document
File TitleMarch 6, 2007
AuthorTheda Kenney
File Modified0000-00-00
File Created2023-10-07

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