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
1.–5. rezultāts no 100.
42. lappuse
... represented , or promoted as an OTC daytime sedative ( or any similar or related indication ) is regarded as a new drug within the meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act for which an approved new drug ...
... represented , or promoted as an OTC daytime sedative ( or any similar or related indication ) is regarded as a new drug within the meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act for which an approved new drug ...
43. lappuse
... represented , or prompted for use as an aphrodisiac is regarded as a new drug within the meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act , ( the act ) , for which an approved new drug application under section ...
... represented , or prompted for use as an aphrodisiac is regarded as a new drug within the meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act , ( the act ) , for which an approved new drug application under section ...
44. lappuse
... represented , or promoted as a topically applied hormone - containing product for drug use , with the excep- tion of those hormones identified in paragraph ( e ) of this section , is re- garded as a new drug within the mean- ing of ...
... represented , or promoted as a topically applied hormone - containing product for drug use , with the excep- tion of those hormones identified in paragraph ( e ) of this section , is re- garded as a new drug within the mean- ing of ...
45. lappuse
... represented , or promoted for the treatment of boils is regarded as a new drug within the meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated ...
... represented , or promoted for the treatment of boils is regarded as a new drug within the meaning of section 201 ( p ) of the Federal Food , Drug , and Cosmetic Act ( the act ) , for which an approved application or abbreviated ...
46. lappuse
... represented , or pro- moted for use as an anticholinergic is regarded as a new drug within the meaning of section 201 ( p ) of the Fed- eral Food , Drug , and Cosmetic Act , for which an approved new drug applica- tion under section 505 ...
... represented , or pro- moted for use as an anticholinergic is regarded as a new drug within the meaning of section 201 ( p ) of the Fed- eral Food , Drug , and Cosmetic Act , for which an approved new drug applica- tion under section 505 ...
Saturs
279 | |
285 | |
290 | |
299 | |
310 | |
331 | |
339 | |
340 | |
223 | |
236 | |
238 | |
239 | |
240 | |
256 | |
257 | |
262 | |
263 | |
265 | |
270 | |
275 | |
351 | |
483 | |
588 | |
593 | |
696 | |
699 | |
761 | |
826 | |
865 | |
890 | |
911 | |
949 | |
Citi izdevumi - Skatīt visu
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