C.F.R. » Title 21 » CHAPTER II—DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE › PART 1315—IMPORTATION AND PRODUCTION QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE › Subpart C—Individual Manufacturing Quotas

21 C.F.R. § 1315.21

Individual manufacturing quotas

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The Administrator shall, on or before December 1 of each year, fix for and issue to each person registered to manufacture in bulk ephedrine, pseudoephedrine, or phenylpropanolamine who applies for a manufacturing quota an individual manufacturing quota authorizing that person to manufacture during the next calendar year a quantity of that chemical. Any manufacturing quota fixed and issued by the Administrator is subject to his authority to reduce or limit it at a later date pursuant to § 1315.26 and to his authority to revoke or suspend it at any time pursuant to §§ 1301.36, 1309.43, 1309.44, or 1309.45 of this chapter.

[72 FR 37448, July 10, 2007, as amended at 88 FR 60143, Aug. 31, 2023]
Notes of Decisions
Cited in 1 case, 2008–2008 · leading case: United States v. 662 Boxes of Ephedrine, 590 F. Supp. 2d 703 (D.N.J. 2008).
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United States v. 662 Boxes of Ephedrine, 590 F. Supp. 2d 703 (D.N.J. 2008). “” 21 C.F.R. § 1315.21 . Claimants allege that “the DEA finalized its assessment of the annual needs needed to determine the 2008 individual manufacturing .”
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