21 CFR §1315.22
Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
Any person who is registered to manufacture ephedrine, pseudoephedrine, or phenylpropanolamine and who desires to manufacture a quantity of the chemical must apply on DEA Form 189 for a manufacturing quota for the quantity of the chemical and shall state separately for each subcategory, as defined in § 1315.07, each quantity of such chemical. Copies of DEA Form 189 may be obtained from the Office of Diversion Control Web site, and must be filed (on or before April 1 of the year preceding the calendar year for which the manufacturing quota is being applied) with the UN Reporting & Quota Section, Diversion Control Division, Drug Enforcement Administration. See the Table of DEA Mailing Addresses in § 1321.01 of this chapter for the current mailing address. A separate application must be made for each chemical desired to be manufactured. The applicant must state the following:
- (a)The name and DEA Chemical Code Number, as set forth in part 1310 of this chapter, of the chemical.
- (b)For the chemical in each of the current and preceding 2 calendar years,
- (c)For the chemical in the next calendar year,
- (1)The desired individual manufacturing quota; and
- (2)Any additional factors that the applicant finds relevant to the fixing of the individual manufacturing quota, including any of the following:
- (i)The trend of (and recent changes in) the applicant's and the national rates of net disposal.
- (ii)The applicant's production cycle and current inventory position.
- (iii)The economic and physical availability of raw materials for use in manufacturing and for inventory purposes.
- (iv)Yield and stability problems.
- (v)Potential disruptions to production (including possible labor strikes).
- (vi)Recent unforeseen emergencies such as floods and fires.