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3. Particulate-matter content of 11 cephalosporin injections: conformance with USP limits. Parkins DA; Taylor AJ Am J Hosp Pharm; 1987 May; 44(5):1111-8. PubMed ID: 3605122 [TBL] [Abstract][Full Text] [Related]
4. Comparison of methods for detection of particulate matter in large-volume perenterals. Blanchard J; Thompson CM; Schwartz JA Am J Hosp Pharm; 1976 Feb; 33(2):144-50. PubMed ID: 1258874 [TBL] [Abstract][Full Text] [Related]
6. Evaluation of acceptance criteria for particulate limits for small-volume parenteral products. Tsuji K; Lewis AR J Pharm Sci; 1978 Jan; 67(1):50-5. PubMed ID: 619115 [TBL] [Abstract][Full Text] [Related]
7. Application of improved standardization methods and instrumentation in the USP particulate test for SVI. Barber TA; Lannis MD; Williams JG; Ryan JF J Parenter Sci Technol; 1990; 44(4):185-203. PubMed ID: 2213427 [TBL] [Abstract][Full Text] [Related]
8. Particulate matter assessment of a clinical investigation on filtration and infusion phlebitis. Schroeder HG; DeLuca PP Am J Hosp Pharm; 1976 Jun; 33(6):543-6. PubMed ID: 1274972 [TBL] [Abstract][Full Text] [Related]
9. Standards for particulate matter in all parenteral drug products. Jeffrey LP; Pinkus TF Am J Hosp Pharm; 1976 Sep; 33(9):879-80. PubMed ID: 984053 [No Abstract] [Full Text] [Related]
10. [Fifth supplement to the United States Pharmacopoeia XIX and National Formulary XIV]. Montanari L Boll Chim Farm; 1979 Oct; 118(10):585-93. PubMed ID: 553525 [No Abstract] [Full Text] [Related]
11. The efficacy of antimicrobial agents in parenteral products assessed by the USP XIX method compared to the USP XVIII method. Tan TG; Wilson RC J Parenter Drug Assoc; 1980; 34(6):431-5. PubMed ID: 7007603 [No Abstract] [Full Text] [Related]
12. [A comparison of the assay regulations for sterility testing between the USP XIX and the European Pharmacopoeia (author's transl)]. Seyfarth H Zentralbl Bakteriol Orig B; 1975 Jul; 160(4-5):432-42. PubMed ID: 811006 [TBL] [Abstract][Full Text] [Related]
14. The potential impact of usp general chapter <797> on procedures and requirements for the preparation of sterile radiopharmaceuticals. Hung JC J Nucl Med; 2004 Jun; 45(6):21N-6N. PubMed ID: 15181115 [No Abstract] [Full Text] [Related]
15. Particulate matter in four reconstituted cephalosporin injections. Kilarski DJ; Visconti JA; Frank SG Am J Hosp Pharm; 1983 Apr; 40(4):619-23. PubMed ID: 6846372 [TBL] [Abstract][Full Text] [Related]
16. Particulate matter test in small volume parenterals: critical aspects in sampling methodology. Pavanetto F; Conti B; Genta I; Ponci R; Montanari L; Grassi M Farmaco; 1989 Jun; 44(6):633-43. PubMed ID: 2803449 [TBL] [Abstract][Full Text] [Related]
17. Problems of particulate matter in sterile solid products for injection. Hammer HF Bull Parenter Drug Assoc; 1974; 28(5):205-16. PubMed ID: 4421783 [No Abstract] [Full Text] [Related]
18. Particulate matter in small volume parenterals: evaluation of some technological and analytical aspects. Cirannni Signoretti E; Montanari I; Neri G; De Sena C; Alimonti S Boll Chim Farm; 1989 Feb; 128(2):65-70. PubMed ID: 2775519 [TBL] [Abstract][Full Text] [Related]
19. Quantitative estimation of particulate matter in pharmaceutical preparations intended for intravenous administration. Bikhazi AB; Shiatis JA; Haddad AF J Pharm Sci; 1977 Feb; 66(2):181-6. PubMed ID: 839413 [TBL] [Abstract][Full Text] [Related]
20. Challenges and scientific issues in the standardization of botanicals and their preparations. United States Pharmacopeia's dietary supplement verification program--a public health program. Srinivasan VS Life Sci; 2006 Mar; 78(18):2039-43. PubMed ID: 16516244 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]