Current through Register Vol. 71, No. 52, December 27, 2024
Rule 22-B1332 - DRUG MANUFACTURERS AND DISTRIBUTORS FEES1332.1The licensure fees for drug manufacturers and distributors located within the District of Columbia are as follows:
(c) Duplicate certificate 20.00(d) License validation 20.001332.2The registration fees for drug manufacturers and distributors located outside the boundaries of the District of Columbia are as follows:
(c) Duplicate certificate 20.00 *These fees are mandated by the Omnibus Budget Support Act of 1994, § 501(b), effective June 14, 1994 (D.C. Law 10-128).
D.C. Mun. Regs. tit. 22, r. 22-B1332
Final Rulemaking published at 42 DCR 5016, 5017 (September 1, 1995); as amended by Final Rulemaking published at 53 DCR 10055 (December 22, 2006)Authority: Section 19(a)(3) of the District of Columbia Pharmacist and Pharmacy Regulation Act of 1980, effective September 16, 1980 (D.C. Law 3-98; D.C. Official Code § 47-2885.18.01(a)(3)); the District of Columbia Uniform Controlled Substances Act of 1981, effective August 5, 1981 (D. C. Law 4-29; D.C. Official Code § 48-901.01); Mayor's Order 98-48, dated April 15, 1998; Section 4902 of the Fiscal Year 2002 Budget Support Act of 2001, effective October 3, 2001 (D.C. Law 14-28; D.C. Official Code § 7-731); Section 15 of the District of Columbia Drug Manufacture and Distribution Licensure Act of 1990, effective June 13, 1990 (D.C. Law 8-137; D.C. Official Code § 48-714(a)); and Mayor's Order 98-88, dated May 29, 1998.