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- CHAPTER I: FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
- CHAPTER II: DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE
- CHAPTER III: OFFICE OF NATIONAL DRUG CONTROL POLICY
CHAPTER II: DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE
PART 1315: IMPORTATION AND PRODUCTION QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE
Subpart B: Assessment of Annual Needs
21 CFR 1315.13 - Adjustments of the assessment of annual needs.
Subpart C: Individual Manufacturing Quotas
21 CFR 1315.22 - Procedure for applying for individual manufacturing quotas.
21 CFR 1315.26 - Reduction in individual manufacturing quotas.
21 CFR 1315.23 - Procedure for fixing individual manufacturing quotas.
21 CFR 1315.27 - Abandonment of quota.
21 CFR 1315.24 - Inventory allowance.
21 CFR 1315.21 - Individual manufacturing quotas.
21 CFR 1315.25 - Increase in individual manufacturing quotas.
Subpart D: Procurement and Import Quotas
21 CFR 1315.32 - Obtaining a procurement quota.
21 CFR 1315.34 - Obtaining an import quota.
21 CFR 1315.36 - Amending an import quota.
21 CFR 1315.30 - Procurement and import quotas.
21 CFR 1315.33 - Power of attorney.
Subpart E: Hearings
21 CFR 1315.56 - Request for hearing or appearance; waiver.
21 CFR 1315.50 - Hearings generally.
21 CFR 1315.58 - Burden of proof.
21 CFR 1315.52 - Purpose of hearing.
21 CFR 1315.60 - Time and place of hearing.
21 CFR 1315.54 - Waiver or modification of rules.
