{"data":{"id":"us-ne/neb.-rev.-stat.-38-2807.01","jurisdiction":"us-ne","citation":"Neb. Rev. Stat. § 38-2807.01","heading":"Neb. Rev. Stat. § 38-2807.01","body":"Bioequivalent means drug products: (1) That are legally marketed under regulations promulgated by the federal Food and Drug Administration; (2) that are the same dosage form of the identical active ingredients in the identical amounts as the drug product prescribed; (3) that comply with compendial standards and are consistent from lot to lot with respect to (a) purity of ingredients, (b) weight variation, (c) uniformity of content, and (d) stability; and (4) for which the federal Food and Drug Administration has established bioequivalent standards or has determined that no bioequivalence problems exist.","path":["NE Code","Chapter 38"],"source_url":"https://nebraskalegislature.gov/laws/statutes.php?statute=38-2807.01","current_through":"2026-08-14","vintage":"open-us-law v2026.08, retrieved 2026-09-14","retrieved_at":"2026-09-14T18:32:21Z","sha256":"699c7cd4e29bf7174c39f5407cc730853352ab87b1c850fd6780275422d3892f","source_id":"us-ne","stale":false,"prev":"us-ne/neb.-rev.-stat.-38-2807","next":"us-ne/neb.-rev.-stat.-38-2807.02"},"notice":"GroundRules: Original legal text. Not legal advice."}