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, 1965 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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Página 20
... manufacture , transportation , storage , or wholesale or retail distribution of veterinary drugs and is to be sold ... manufacturing history of the package of the drug ; Provided , however , That in the case of containers too small or ...
... manufacture , transportation , storage , or wholesale or retail distribution of veterinary drugs and is to be sold ... manufacturing history of the package of the drug ; Provided , however , That in the case of containers too small or ...
Página 23
... manufacture . A drug in a bulk package ( except tablets , capsules , or other dosage unit forms ) or a device ... manufacturing , processing , or repacking ” is immediately supplemented by the words " in the prep- aration of a new ...
... manufacture . A drug in a bulk package ( except tablets , capsules , or other dosage unit forms ) or a device ... manufacturing , processing , or repacking ” is immediately supplemented by the words " in the prep- aration of a new ...
Página 37
... manufacturing processes or controls . The Director of the Bureau of Medicine , the Director of the Division of New Drugs , and the Di- rector of the Division of Veterinary Medi- cine are authorized to notify applicants of supplements to ...
... manufacturing processes or controls . The Director of the Bureau of Medicine , the Director of the Division of New Drugs , and the Di- rector of the Division of Veterinary Medi- cine are authorized to notify applicants of supplements to ...
Página 43
... manufacturing The Director of processes or controls . the Bureau of Medicine , the Director of the Division of New Drugs , and the Di- rector of the Division of Veterinary Medi- cine are authorized to notify applicants of supplements to ...
... manufacturing The Director of processes or controls . the Bureau of Medicine , the Director of the Division of New Drugs , and the Di- rector of the Division of Veterinary Medi- cine are authorized to notify applicants of supplements to ...
Página 43
... manufacturers , packers , and distributors of glandular prepara- tions . Notice to manufacturers , packers , and distributors of drugs for internal use which contain mineral oil . Disposition of incubator reject eggs . Notice to ...
... manufacturers , packers , and distributors of glandular prepara- tions . Notice to manufacturers , packers , and distributors of drugs for internal use which contain mineral oil . Disposition of incubator reject eggs . Notice to ...
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0.2 percent 52 Stat acetate acid added alcohol amended Amprolium artificial bacitracin bear the statement blank being filled calcium certification cheese chickens chloride Chlortetracycline colby cheese color additive combination copolymer corn sirup Cosmetic Act curd D&C Red definition and standard dried ethylene exceed exemption extract Federal Food flavoring flour food additive Food and Drug fruit glucose sirup glycol grams gredients Hygromycin ingredients specified label shall bear label statement manufacturing ment method prescribed methyl milligrams milliliters million mixture Nystatin optional ingredients oxide Oxytetracycline oysters package packing pasteurized percent by weight Polyoxyethylene Polysorbate 60 potassium prepared principal ingredient process cheese quantity regulations resins safely salt sample shrimp sieve sirup skim milk sodium solids sorbitan specified in paragraph spice standard of identity statement of optional subparagraph Subpart substances sugar sulfate tion titanium trichloride tolerances for residues tylosin units