{"data":{"id":"us-va/18vac110-20-321","jurisdiction":"us-va","citation":"18VAC110-20-321","heading":"Compounding","body":"A. The compounding of both sterile and nonsterile drug products by a pharmacy that does not share the same physical space with an outsourcing facility shall be performed in accordance with USP-NF compounding standards and § 54.1-3410.2 of the Code of Virginia.\n\nB. The compounding of sterile drug products by an outsourcing facility or by a pharmacy sharing the same physical space with an outsourcing facility shall be performed in accordance with current good manufacturing practices under § 501(a)(2)(B) of the Federal Food, Drug, and Cosmetic Act (21 USC § 351(a)(2)(B)).","path":["Title 18. Professional And Occupational Licensing","Agency 110. Board of Pharmacy","Chapter 20. Regulations Governing the Practice of Pharmacy","Part VI. Labeling and Packaging Standards for Prescriptions"],"source_url":"https://law.lis.virginia.gov/admincode/title18/agency110/chapter20/section321/","current_through":"2026 Regular Session (effective July 1, 2026)","vintage":"","retrieved_at":"2026-09-14T04:52:58Z","sha256":"17558e41bb33f8ce90a1d36e6c9f610048a40fb7a42fd8749991828cb801fcfc","source_id":"us-va-vac","stale":false,"prev":"us-va/18vac110-20-320","next":"us-va/18vac110-20-322"},"notice":"GroundRules: Original legal text. Not legal advice."}