处方药调配容器的要求；生效日期的延缓 - Suppr | 超能文献

处方药调配容器的要求；生效日期的延缓 - Suppr | 超能文献

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1

Requirements for dispensing containers for prescription drugs; stay of effective date.处方药调配容器的要求；生效日期的延缓

Fed Regist. 1979 Aug 10;44(156):47042-3.

2

Prescription drug dispensing container requirements: final rule.

Fed Regist. 1978 Aug 25;43(166):37985-9.

3

Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; policies, requirements, and administrative procedures; delay of effective date. Final rule; delay of effective date.1987年《处方药营销法》；1992年《处方药修正案》；政策、要求及行政程序；生效日期延迟。最终规则；生效日期延迟。

Fed Regist. 2004 Feb 23;69(35):8105-7.

4

Relief in tamper-resistant packages.防篡改包装中的缓解措施。

FDA Consum. 1983 Feb;17(1):12-6.

5

Prescription Drug Marketing Act of 1987; Prescription Drug Amendments of 1992; policies, requirements, and administrative procedures; delay of effective date; reopening of administrative record. Food and Drug Administration, HHS. Final rule; delay of effective date; reopening of administrative record.

Fed Regist. 2000 May 3;65(86):25639-41.

6

Human and veterinary drugs: good manufacturing practices and proposed exemptions for certain OTC products.人用和兽用药品：良好生产规范及某些非处方药产品的拟议豁免规定。

Fed Regist. 1978 Sep 29;43(190 Pt 2):45013-89.

7

Drugs, codes, standards, and other incompatible things in the dark.黑暗中的药物、编码、标准及其他不相容之物。

MD Comput. 2001 Jan-Feb;18(1):45-6.

8

Hazard: Sav-a-life oxygen containers.危险：救生氧气容器。

Health Devices. 1972 Jul-Aug;1(11):265.

9

Food and Drug Administration--Prescription drug products; patient package inserts requirements. Final rule.食品药品监督管理局——处方药产品；患者用药指导手册要求。最终规则。

Fed Regist. 1980 Sep 12;45(179 Pt 2):60754-84.

10

Content and format for labeling for human prescription drugs; amendment of effective date for certain biological products--Food and Drug Administration. Final rule.人用处方药标签的内容和格式；某些生物制品生效日期的修订——食品药品监督管理局。最终规则。

Fed Regist. 1981 Jan 23;46(15 pt 1):7271-3.