BIOAVAILABILITY AND BIOEQUIVALENCE

被引：15

作者：

SKELLY, JP ^{[1
]}

机构：

[1] US FDA,ROCKVILLE,MD 20852

来源：

JOURNAL OF CLINICAL PHARMACOLOGY | 1976年 / 16卷 / 10期

关键词：

D O I：

10.1177/009127007601601013

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：539 / 545

页数：7

共 12 条

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[2]

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[3]

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[4] LOS OF SENSITIVITY IN DISTINGUISHING REAL DIFFERENCES IN DISSOLUTION RATES DUE TO INCREASING INTENSITY OF AGITATION [J].

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LEVY, G ;

HAYES, BA .

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[6] EFFECT OF CERTAIN TABLET FORMULATION FACTORS ON DISSOLUTION RATE OF ACTIVE INGREDIENT .1. IMPORTANCE OF USING APPROPRIATE AGITATION INTENSITIES FOR IN VITRO DISSOLUTION RATE MEASUREMENTS TO REFLECT IN VIVO CONDITIONS [J].

LEVY, G .

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[7] SOLUTION RATE OF THEOPHYLLINE SALTS AND EFFECTS FROM ORAL ADMINISTRATION [J].

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[8] COMPARATIVE DISSOLUTION RATES OF WEAK ACIDS AND THEIR SODIUM SALTS [J].

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[9]

SCHMIDT AM, 1975, FED REG 26142, V40

[10] PHARMACOLOGICAL RESPONSE DATA FOR COMPARATIVE BIOAVAILABILITY STUDIES OF CHLORPROMAZINE ORAL DOSAGE FORMS IN HUMANS .1. PUPILLOMETRY [J].

SMOLEN, VF ;

MURDOCK, HR ;

STOLTMAN, WP ;

CLEVENGER, JW ;

COMBS, LW ;

WILLIAMS, EJ .

JOURNAL OF CLINICAL PHARMACOLOGY, 1975, 15 (11-1) :734-751

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