There is a newer version
of
this Statute
2018 Nebraska Revised Statutes
Chapter 38 - HEALTH OCCUPATIONS AND PROFESSIONS
38-2807.01 Bioequivalent, defined.
Universal Citation: NE Code § 38-2807.01 (2018)
38-2807.01. Bioequivalent, defined.
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.
Source
- Laws 1977, LB 103, § 2;
- Laws 1983, LB 476, § 21;
- Laws 1989, LB 342, § 36;
- Laws 1996, LB 1044, § 720;
- Laws 1998, LB 1073, § 148;
- Laws 2001, LB 398, § 76;
- Laws 2003, LB 667, § 15;
- Laws 2005, LB 382, § 11;
- Laws 2007, LB296, § 622;
- Laws 2007, LB463, § 1232;
- R.S.1943, (2009), § 71-5402;
- Laws 2015, LB37, § 61;
- R.S.1943, (2016), § 38-28,110;
- Laws 2017, LB481, § 3.
Disclaimer: These codes may not be the most recent version. Nebraska may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
This site is protected by reCAPTCHA and the Google
Privacy Policy and
Terms of Service apply.
