Pharmaceutical Technology BioPharm - May 2025

Pharmaceutical Technology BioPharm - May 2025

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24 Pharmaceutical Technology ® | BioPharm International ® Trends in Manufacturing May 2025 PharmTech.com COMPOUNDING formats in labeling (Table I) that do not follow the FDA format described above. For example, metopro- lol tartrate (Lopressor) is an immediate-release beta blocker that is dosed twice daily; metoprolol succi- nate (Toprol XL) is an extended-release metoprolol preparation formulated for once-daily dosage. Sec- ondar y labeling on metoprolol succinate products (37–39) references metoprolol tartrate to aid in tran- sitioning patient dosage. Potassium phosphates injec- tion (policy-exception drug) is labeled as phosphorus mmol/mL and potassium mEq/mL on the primary label and mg/mL amounts of potassium phosphate monobasic and potassium phosphate dibasic equiva- lent amounts of potassium and phosphate on the side panel (40,41). Succinylcholine labeling may be incon- sistent or different format (e.g., same concentration products may be labeled as total drug mg/vial. (42– 44). These labels were likely approved before the salt policy was implemented and have not been updated. Summary Par t one of t his series addresses pharmaceutica l principles including terminology, regulations, and dosage form labeling in compounded preparations. Ty pes of dr ugs are identif ied. Non-salt (covalent) drugs and salt (ionic) drugs are primary groups; cer- tain salt drugs are further grouped as policy-excep- tion salts. Policy-exception salts are dosed as non-salt drugs including their molecule counterions; labeling must identif y the equivalent active drug amounts. Forms of drugs are also identified. Drug forms may be solids or liquids; they may be bulk drugs or drugs in mixtures; mixtures may include solutions, mix- tures of solids, and commercial products (e.g., tab- lets). Table II summarizes the drug types, dosage ra- tionale, forms, active moiety identification, primary labeling, and secondary labeling. The USP salt policy, historical precedent, and identified exceptions are the bases for these requirements; note significant la- beling differences between salt drugs and policy-ex- ception salts. Problems associated with the above are identified. Effects resulting from misunderstanding of drug salt principles may include overdosing or un- derdosing of dosage form active moiety. Mislabeling of dosage form content is also possible; attention to detail is critical. Labeling may have variations for a variety of reasons. Caref ul reading of commercial product labeling with good understanding of prin- ciples is mandatory for compounded product appli- cations. Acknowledgments Comments from Alan M. Mancini, RPh, pharmaceutical educator; Richard Poska, RPh, Flexo CMC Consulting; Jan M. Keresztes, RPh, PharmD, pharmaceutical educa- tor; and William R. Porter, PhD, pharmaceutical educa- tor and principal scientist, Peak Process Performance Partners, are greatly appreciated. References 1. A n se l , H.C. Ph a r m aceut ic a l Ca lc u l at ion s, 1 4t h ed it ion. Wolter s K luwer/ L ippi ncot t , Wi l l i a m s, & Wi l k i n s, Ph i l- adelph ia, PA, 2013. 2. Tei xei ra, M.G. a nd Zat z, J.L . Phar maceut ical Calculat ions, 5t h edit ion. Joh n Wi ley & Sons, Hoboken NJ, 2017. 3. A l len , L .V., Jr. Phar maceut ical Compounding Calculat ion s in T he A r t , Science, and Technology of Phar maceut ical Com- p o un din g, 6t h e d . A me r ic a n Ph a r m a c i s t s A s s o c i a t ion , Wash i ng ton, D.C., 2020. 4. IC H . Q 9 (R 1) Q u a l i t y R i s k M a n a g e m e n t (IC H , Ja nu a r y 2023). ht t ps://d at aba se.ich.org/sites/defau lt/f i les/ ICH _ Q 9 % 2 8R 1% 29 _G u i d e l i ne _ St e p 4 _ 202 3 _ 01 26 _ 0.p d f (a c- cessed Nov. 1, 202411-1-24). 5. ASHP. Compounding Frequent ly Asked Questions. ASHP. or g. S e pte m b e r 2016. ht t ps:// w w w.a s hp.or g /-/me d i a/ a s s e t s/a d v o c a c y-i s s u e s/d o c s/c o m p o u n d i n g- g u i d a n c - e s -f r e q u e n t l y-a s k e d- q u e s t i o n s . a s h x? l a= e n (a c c e s s e d Nov.1, 2024). 6. FDA. Compounding and the FDA. Questions and Answers. F DA . go v. Nov. 15 , 202 4. ht t ps:// w w w.fd a.gov/d r ugs/ hu- m a n- d r u g- comp ou nd i n g /comp ou nd i n g-a nd-f d a- q ue s- t ions-a nd-a nswers (accessed Nov.1, 2024). 7. P l u t a , P. L . C o m p o u n d i n g O v e r v i e w : P r i m a r y C o n s i d- e r a t i o n s i n t h e Wo r k p l a c e . P h a r m a c e u t i c a l Te c h n o l - o g y, 202 4 4 8 (2) p1 8-2 2 . ht t ps:// w w w.ph a r m t e c h .c om/ TABLE II. Drug dosage and labeling summary. 503A pharmacy labeling is also regulated by state agencies. Drug Type Description Drug Form Active Moiety Dosage Primary Label Secondary label Non-salt (covalent) Active moiety same as (bulk drug) Bulk drug or drug mixture Drug amount Drug amount Drug amount Salt (ionic) Active moiety is drug-ion Drug-ion amount Drug-ion amount Drug-ion amount and equivalent bulk drug amount Policy-exception salt (ionic) Active moiety dosage is drug-ion + drug counterion Drug amount Drug ion + counterion amount Drug amount and equivalent drug-ion amount

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