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By Kleemann A., Engel J.

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1972). DOS 2 319 834 (CarloErba;appl. 1973; I-prior. 1972). I-prior. 1972). GB 1 361 967 (CarloErba;appl. J. Med. (EJMCA5)15,157 (1980). (CHBEAM)99,364(1966). :J. (JOCEAH)26,129 (1961). 5443-991 MF: C4,H53NOl, . 34 I Aclorubicin Aclatonium napadidate A 35 By fermentation of Streptomyces galilaeus MA 144-M1 (ATCC 31 13); separation of aclacinomycin A and B by column chromatography. Reference(s): DOS 2 532 568 (Zaidanhojin Biseibutsu Kagaku Kenkykai; appl. 1975; J-prior. 1974). 1976; J-prior. 1974).

20h. ; USA-prior. 1993). ; appl. 1995; USA-prior. 1994). 1995; USA-prior. 1993). DE 3 016 289 (Henkel KG; D-prior. 1980). BE896 453 (1st. Gentili s. p. ; appl. 1983; I-prior. 1983). BE903 513 (1st. Ccntili s. p. ; appl. 1985; I-prior. 1984). EP 494 844 (1st. Gentili s. p. ; appl. 1992; I-prior. 1991). US 4 621 077 (1st. Gentili s. p. 1984; I-prior. 1982). 1991; USA-prior. 1990). 1990; USA-prior. 1989). ; CA-prior. 1997). Formulation(s): amp. 5 mg, 10 mg; tabl. 5 mg, 10 mg, 40 mg (as sodium salt) I A 54 Alfacalcidol Trade Name(s): D: Fosamax (Merck Sharp & Dohme) GB: Fosamax (Merck Sharp & Dohme) I: Adronat (Neopharmed) Alendros (Gentili) Dronal (Sigmatau) Fosamax (Merck Sharp & Dohme) Onclast (Banyu) J: Alfacalcidol ATC: Use: (la-Hydroxycholecalciferol; la-Hydroxy-vitamin D,) 'Teiroc (Teijin) USA: Fosamax (Merck Sharp &.

1972; USA-prior. 1971). ; appl. 1979; USA-prior. 1979). 1977; USA-prior. 1976). DOS 2 923 953 (Upjohn; appl. 1979; USA-prior. 1978). G. : Tetrahedron Lett. (TELEAY) 1973, 3649. 1977; prior. 1976). pharmaceutical formulation: JP-appl. 78 136 512 (Chugai; appl. 1977). 1979; J-prior. 1977) use as anti-inflammatory: FX 2 389 377 (J. Brohult, appl. 1977). Formulation(s): amp. 002 mg; cps. 0025 mg, 1 mg; inj. ) 55 A 56 Alfaxalone ride etherote alfaxalone (I) lead tetraacetate Alfodolane ocetote (4. HBr.

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