Code of Federal Regulations: Containing a Codification of Documents of General Applicability and Future Effect as of December 31, 1948, with Ancillaries and IndexDivision of the Federal Register, the National Archives, 1998 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
No grāmatas satura
6.–10. rezultāts no 64.
45. lappuse
... meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated application under section 505 of the act and part 314 of this chapter is required for marketing ...
... meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated application under section 505 of the act and part 314 of this chapter is required for marketing ...
47. lappuse
... abbreviated application under sec- tion 505 of the act and part 314 of this chapter is required for marketing . In the absence of an approved new drug application or abbreviated new drug application , such product is also mis- branded ...
... abbreviated application under sec- tion 505 of the act and part 314 of this chapter is required for marketing . In the absence of an approved new drug application or abbreviated new drug application , such product is also mis- branded ...
48. lappuse
... meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated application under section 505 of the act and part 314 of this chapter is required for marketing ...
... meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated application under section 505 of the act and part 314 of this chapter is required for marketing ...
50. lappuse
... meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated application under section 505 of the act and part 314 of this chapter is required for marketing ...
... meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated application under section 505 of the act and part 314 of this chapter is required for marketing ...
60. lappuse
... meaning of sec- tion 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated application under section 505 of the act and part 314 of this chapter is required for marketing ...
... meaning of sec- tion 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated application under section 505 of the act and part 314 of this chapter is required for marketing ...
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Bieži izmantoti vārdi un frāzes
abbre abbreviated application abbreviated new drug acid active ingredient adverse drug experience agency amended antibiotic application or abbreviated bacitracin bioavailability bioequivalence cation Center for Drug certification chapter clinical hold clinical investigation conducted control number copy Cosmetic Act digoxin dosage form dose Drug Administration drug application Drug Evaluation drug prod drug product Drug products containing drug substance Evaluation and Research Federal Food Food and Drug graph gredients hearing hydrochloride identified information requirements ap insulin intended inves investigational new drug labeling manufacturer marketing meet ment milligrams milliliters misbranded neomycin notice oral dosage orphan drug OTC drug product package paragraph percent person plication polymyxin proposed protocol recognized as safe reference listed drug request safe and effective safety section 502 Sodium sponsor statement submission Subpart sulfate tained tigational tion tive treatment treatment IND vestigational viated warning