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Generic promethazine codeine cough syrup by mouth) and codeine cough syrup (promethazine syrup) (oral tablets) in all or a combination of the following: dose; strength; type; pack size; and date of manufacture. (13) Any oral prescription drug which contains an inactive ingredient (other than a placebo, as non-drug delivery device) in amounts which are not higher than the minimum amounts recommended by Food and Drug Administration for the active ingredient. (14) Any oral prescription drug which contains acetaminophen in amounts not equivalent to or lower than those in Schedule II, III, IV, V, or VI of 21 CFR Part 121 this Esomeprazole over the counter canada chapter. (15) Any oral narcotic drug which contains benzodiazepines except in accordance with paragraph (d) of this section or in accordance generic promethazine codeine cough syrup with 23 CFR 441.38 Order xenical online canada and except in a dosage form which does not contain more than 50 mg of benzodiazepines per dose or a 10% alcohol content, as described in the following non-labeled drug product labeling: * Buprenorphine dihydrochloride (Subsys (d)) Citation: Authority: 47 FR 43865, Aug. 15, 1982, unless otherwise noted. Redesignated and Restated 21 CFR 441.31. Revision date: March 31, 1992. Effective Date: 01-01-2004. (a) If it is necessary to use a drug or preparation to control an animal behavior which is caused or made more likely by the presence of a substance or an agent, including but not limited to pain medications, tranquilizers, anticonvulsants, sedatives, depressants, hallucinogens, and sedatives of other types, which is likely to adversely affect the behavior of animal, it is necessary to do so in a manner which, either alone, or in combination, does not increase the negative influence of drug on the animal's capacity to learn and avoid distress. (b) When considering the use of a drug or preparation, its influence on performance, behavior, health, or welfare of an animal, any other relevant factor of substance, compound, or mixture, the prescriber must consider following considerations: (1) The degree to which drug or preparation affects the performance, behavior, health, or welfare of an animal. (2) The extent to which effects of the drug or preparation are transmitted to other animals than those in the same or other treatment groups. (3) The degree to which animal's condition and the effect of drug or preparation on its health are worsened or improved. (4) The amount of drug or preparation administered, and the degree to which it is administered. (5) The amount of food given to the animal. (6) The nature and rate of administration. (7) The quantity, frequency, and dosage of other medical surgical treatment the drug or preparation is intended to be effective for. (8)(i) Any effect of the drug or preparation on a disease of an animal. (ii) Any effect of the drug or preparation on an organism that is not animal. (9) Whether there is a safe and practical alternatives to the drug or preparation. (10) Any other relevant consideration. [53 FR 28160, June 30, 1988, as amended at 73 FR 37198, June 30, 2008] §417.43 Application. (a) A hi tech promethazine codeine canada veterinarian must submit an application, which include each of the following: (1) For drug preparations not specified under §417.37(a)(2): (i) An unopened container to be submitted with the drug. (ii) The manufacturing process or method by which the drug is administered/used to animals. (iii) The identity of animals treated with the drug, including but not limited to method and duration of treatment. (iv) A description of the manner in which and quantities of active pharmaceutical ingredients are present in the drug. (v) Two photographs of an unweaned neonate for each dose of the drug or preparant administered to the animal. (vi) The name, address, and telephone number of an individual to contact for further information. (vii) The information requested under §417.34(c) and (d). (2) For drug preparations specified under §417.37(a)(2): (i) An unopened container to be submitted with the drug. (ii) The manufacturing process or method by which the drug is administered/used.

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