These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 5469814)

  • 1. Objective visual evaluation of the relative content of major and minor defects in tablets and capsules.
    Stone JC
    J Pharm Sci; 1970 Sep; 59(9):1364. PubMed ID: 5469814
    [No Abstract]   [Full Text] [Related]  

  • 2. The study of the applicability of content uniformity and weight variation test--the state of commercial tablets and capsules in Japan.
    Katori N; Aoyagi N; Kojima S
    Chem Pharm Bull (Tokyo); 2001 Nov; 49(11):1412-9. PubMed ID: 11724231
    [TBL] [Abstract][Full Text] [Related]  

  • 3. In vitro evaluation of physiological availability of compressed tablets.
    Wood JH
    Pharm Acta Helv; 1967 Mar; 42(3):129-51. PubMed ID: 4870534
    [No Abstract]   [Full Text] [Related]  

  • 4. "In vitro" dissolution tests for solid oral dosage forms.
    Rees JE
    Boll Chim Farm; 1977 Sep; 116(9):499-505. PubMed ID: 597400
    [No Abstract]   [Full Text] [Related]  

  • 5. New in vitro disintegration and dissolution test method for tablets and capsules.
    Goodhart FW; McCoy RH; Ninger FC
    J Pharm Sci; 1973 Feb; 62(2):304-10. PubMed ID: 4686409
    [No Abstract]   [Full Text] [Related]  

  • 6. Uniformity of content requirements for tablets and capsules.
    Kendall CE; Low GK; Hailey DM
    J Pharm Pharmacol; 1981 Apr; 33(4):197-202. PubMed ID: 6115899
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Particle size limits to meet USP content uniformity criteria for tablets and capsules.
    Rohrs BR; Amidon GE; Meury RH; Secreast PJ; King HM; Skoug CJ
    J Pharm Sci; 2006 May; 95(5):1049-59. PubMed ID: 16552749
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Testing for uniformity: sampling plans in pharmacopeias for weight, volume, and content uniformity.
    Pietra V; Setnikar I
    J Pharm Sci; 1970 Apr; 59(4):530-5. PubMed ID: 5440682
    [No Abstract]   [Full Text] [Related]  

  • 9. [Progress in drug technology in the years 1968 and 1969].
    Chalabala M; Malý J; Burelová A
    Cesk Farm; 1970 Nov; 19(9):332-60. PubMed ID: 4926371
    [No Abstract]   [Full Text] [Related]  

  • 10. Comparison between the U.S.P. 18 and the wet sieving disintegration tests.
    Sandell E; Helmstein I
    Acta Pharm Suec; 1971 Nov; 8(5):549-52. PubMed ID: 5159524
    [No Abstract]   [Full Text] [Related]  

  • 11. Panel discussion: in process control and inspection for quality assurance. II.
    Hofer AJ
    Bull Parenter Drug Assoc; 1968; 22(2):87-90. PubMed ID: 5649571
    [No Abstract]   [Full Text] [Related]  

  • 12. Development of a process control scheme for reduction in weight variation of capsules.
    Das P
    PDA J Pharm Sci Technol; 2007; 61(3):194-203. PubMed ID: 17722486
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Studies on flow properties of powders. IV. Flow properties of tablet granulations and the uniformity of tablet content.
    Kristensen HG
    Dan Tidsskr Farm; 1969; 43(9):213-9. PubMed ID: 5371697
    [No Abstract]   [Full Text] [Related]  

  • 14. Editorial: Dissolution test blossoms.
    Feldmann EG
    J Pharm Sci; 1976 Apr; 65(4):I. PubMed ID: 1271242
    [No Abstract]   [Full Text] [Related]  

  • 15. [Replacement of standard prescription regulations for pills by new regulations for tablets in the GDR (SP edition 1971). 2. Processing of drug combinations from plant extracts].
    Moldenhauer H; Hünerbein B; Krüger H; Kala H
    Pharm Prax; 1973; 5():111-2. PubMed ID: 4718085
    [No Abstract]   [Full Text] [Related]  

  • 16. [Progress in the production and control of tablets. X. On the theoretical basis of compressing].
    Malý J
    Cesk Farm; 1968 Feb; 17(2):94-8. PubMed ID: 4871275
    [No Abstract]   [Full Text] [Related]  

  • 17. Letter: USP content uniformity test.
    Madan PL
    J Pharm Sci; 1976 Jan; 65(1):VIII. PubMed ID: 1255410
    [No Abstract]   [Full Text] [Related]  

  • 18. Characterization of the content uniformity plan.
    Sampson CB; Breunig HL; Comer JP; Broadlick DE
    J Pharm Sci; 1970 Nov; 59(11):1653-5. PubMed ID: 5495497
    [No Abstract]   [Full Text] [Related]  

  • 19. [Technologic control of tablet coatings].
    Dia S; Guyot JC; Traisnel M
    J Pharm Belg; 1973; 28(6):663-80. PubMed ID: 4774837
    [No Abstract]   [Full Text] [Related]  

  • 20. Studies on flow properties of powders. 3. The influence of glidants on the technical properties of tablet granulations.
    Kristensen HG; Jensen VG
    Dan Tidsskr Farm; 1969; 43(9):205-12. PubMed ID: 5371696
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.