21 CFR 558.5 - Requirements for liquid medicated feed
| Cite as | 21 CFR 558.5 |
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10 practice notes
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Human drugs, biological products, and animal drugs; foreign and domestic establishment registration and listing requirements,
...relabelers, or drug product salvagers of certain free-choice feeds, as defined in 21 CFR 510.455, or certain liquid feeds, as defined in 21 CFR 558.5, where the specifications and/or formulas are not published and a feed mill license is required). Proposed Sec. 207.13(f) also clarifies that......
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Part II
...relabelers, or drug product salvagers of certain free-choice feeds, as defined in 21 CFR 510.455, or certain liquid feeds, as defined in 21 CFR 558.5, where the specifications and/or formulas are not published and a feed mill license is required). Proposed Sec. 207.13(f) also clarifies that......
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Agency information collection activities; proposals, submissions, and approvals,
...or no time preparing the FOI summary, the estimated burden hours are 19 hours. Requirements for liquid medicated feeds (Sec. 558.5(i) (21 CFR 558.5(i)). Generally, specific labeling is required to make sure that certain drugs, approved for use in animal feed or drinking water but not in liq......
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Agency Information Collection Activities; Proposed Collection; Comment Request; Reporting Associated With New Animal Drug Applications
...data submissions has created efficiencies for both us and the animal pharmaceutical industry. Finally, Sec. 558.5(i) of our regulations (21 CFR 558.5(i)) describes the procedure for requesting a waiver of the labeling requirements of Sec. 558.5(h) in the event that there is evidence to indi......
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