Agri-Tech, Inc. v. Richardson, 72-1252.
Decision Date | 02 August 1973 |
Docket Number | No. 72-1252.,72-1252. |
Citation | 482 F.2d 1148 |
Parties | AGRI-TECH, INC., a Missouri corporation, Petitioner, v. Elliot L. RICHARDSON, Secretary of Health, Education, and Welfare, and Dr. Charles C. Edwards, Commissioner of Food and Drugs, Respondents. |
Court | U.S. Court of Appeals — Eighth Circuit |
Kirkpatrick W. Dilling, Chicago, Ill., for petitioner.
Howard S. Epstein, Asst. Chief, Consumer Affairs, Antitrust Div., Dept. of Justice, Washington, D. C., for respondents.
Before MATTHES, Senior Circuit Judge, BRIGHT, Circuit Judge, and
Agri-Tech, Inc. has petitioned this court to review an order of the Secretary of Health, Education, and Welfare issued through the Commissioner of Food and Drugs on February 24, 1972, withdrawing approval of New Animal Drug Applications (NADA) Nos. 5-987V and 5-633V, respectively, concerning drugs containing "iodinated casein," or "Protamone," as the active ingredient.1
On January 10, 1973, we heard arguments, and the cause was taken under submission. Two days prior thereto, January 8, 1973, the Supreme Court had granted certiorari in Bentex Pharmaceuticals, Inc. v. Richardson, 463 F.2d 363 (4th Cir. 1972) ; CIBA Corp. v. Richardson, 463 F.2d 225 (3rd Cir. 1972) ; USV Pharmaceutical Corp. v. Richardson, 461 F.2d 223 (4th Cir. 1972) ; Hynson, Westcott & Dunning, Inc. v. Richardson, 461 F.2d 215 (4th Cir. 1972). Directly involved in those cases were the issues posed here. We therefore concluded to withhold our decision until opinions were forthcoming in the above cases. On June 18, 1973, opinions were filed by the Supreme Court and are reported sub nomine Weinberger v. Bentex Pharmaceuticals, Inc., 412 U.S. 645, 93 S.Ct. 2488, 37 L.Ed.2d 235 ; CIBA Corp. v. Weinberger, 412 U.S. 640, 93 S.Ct. 2495, 37 L.Ed.2d 230 ; USV Pharmaceutical Corporation v. Weinberger, 412 U. S. 655, 93 S.Ct. 2498, 37 L.Ed.2d 244 ; Weinberger v. Hynson, Westcott & Dunning, Inc., 412 U.S. 609, 93 S.Ct. 2469, 37 L.Ed.2d 207. Our judgment to delay decision has been vindicated. The Supreme Court opinions, in our view, are dispositive of petitioner's challenge to the withdrawal order.
I. STATUTORY HISTORY AND SCHEME
The statutory history and regulatory scheme are discussed and considered in Weinberger v. Hynson, etc., supra ( ). Therefore, another full recitation of the applicable statutes and regulations is unnecessary. We will, however, discuss the pertinent provisions of the legislation in our consideration of the issues which petitioner continues to urge upon us.
By way of background, petitioner has for approximately 25 years distributed and sold in interstate commerce products for animal feeding purposes containing iodinated casein, also known as Protamone. For some years subsequent to 1945, animal applications of iodinated casein were the subject of new animal drug applications, specifically, NADAs Nos. 5-633V and 5-987V. The applications had been approved by the United States Food and Drug Administration.
In 1962, Congress amended the Food, Drug and Cosmetic Act to expand jurisdiction of the Commissioner of the Food and Drug Administration to allow review of "new drugs" for substantial evidence of both safety and effectiveness. Pub.L. 87-781, 76 Stat. 780. The provision applied equally to human and animal drugs until the amendments in 1968, Pub.L. 90-399, 82 Stat. 342, separated and recompiled the provisions relating to animal drugs. S.Rep.No.1308, 90th Cong., 2d Sess.; 1968 U.S.Code, Cong. and Adm.News, p. 2607 et seq. These separate provisions are, insofar as applicable here, nearly identical.
To effect the provisions of the 1962 amendment, particularly 21 U.S.C. § 355(e), the FDA by notice in 31 Fed. Reg. 9426 on July 9, 1966, announced that the National Academy of Sciences-National Research Council (NAS-NRC) had agreed to assist the FDA in its review of claims of effectiveness for drugs that had been approved from 1938 until October, 1962. All holders of NDAs were directed to submit data to NAS-NRC in order to facilitate the determination whether there was ground for invoking § 505(e) of the Act, and to provide each holder of an approved new-drug application an opportunity to present for the consideration of NAS-NRC the best data available to support the claims.
Petitioner responded to the notice by submitting data for each iodinated casein product on a "Drug Efficacy Study-Form Letter A." According to the data submitted on the forms, Protamone:
In support of these claims petitioner submitted with these Forms A various citations to and reprints of studies allegedly evidencing the claims of effectiveness. The NRC then reviewed these data, and revealed its detailed reasoning on Forms B-1, which appear as a part of the official record filed in the office of the clerk of this court, but not in the Appendix. Apparently, petitioner never received the Forms B-1, but only the Forms B-2, which contain only the NRC's ultimate findings, and the FDA Notice of Hearing, 36 Fed.Reg. 17367, infra, which summarized these findings. We shall review seriatim the supporting data and NRC B-2 conclusions which were given to petitioner.
To support its claim that Protamone improves growth and feathering in turkeys, petitioner submitted only an article cited at 27 Poultry Sci. 670 (1948) entitled "The effect of iodinated casein on moulting turkeys." The conclusion of the NRC as to this claim was "not effective." Under explanatory statements it said: "Induces moulting; no data on growth and feathering." (Emphasis supplied.)
To support its claims that Protamone improves egg production and texture, and growth and feathering in chickens, petitioner cited 33 articles. The Form B-2 from the NRC said
To support its claims that Protamone improves growth and feathering and decreases carcass fat in ducks, petitioner cited four articles. The B-2 form from the NRC said "effective," but said the label's "claims should state `increases daily gain' instead of `improving growth and feathering.'"
To support its claim that Protamone increases milk and butterfat production, growth, fertility and libido in goats and sheep, petitioner cited 14 published articles, attached two unpublished articles and a letter of endorsement from a corporate farm as to goats; as to sheep it cited 24 published articles and attached two unpublished articles. The Forms B-2 from the NRC evaluated iodinated casein as to both goats and sheep as follows:
According to the NRC, "Categories b and c above must have more information before further consideration can be given."
To support the claims Protamone increases milk flow and weaning weights, reduces baby mortality and improves growth, market finish, fertility and libido in swine, petitioner cited 28 articles and attached two articles. The NRC said on the Form B-2,
Supporting its claims that Protamone increases milk and butterfat production, growth, fertility and libido in beef and dairly cattle, petitioner cited nine articles as to beef cattle and as to dairy cattle apparently cited 81 articles, plus attaching nine articles and various letters, advertisements and news items. As to both beef and dairy cattle, the NRC reported on the B-2 forms the following evaluation:
Following this NRC evaluation of the data submitted by petitioner, the Commissioner published on October 8, 1970, at 35 Fed.Reg. 15859 his findings based upon the NRC evaluation. They were:
As to the uses found effective, the NRC and FDA found the label should qualify the claims by informing the user as follows:
This order gave petition...
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...976, 978 (5th Cir.1984); International Nutrition v. U.S. Dept. of Health, 676 F.2d 338, 339 (8th Cir.1982); Agri-Tech, Inc. v. Richardson, 482 F.2d 1148, 1150-51 (8th Cir.1973). "New animal drugs," must be approved by the Food and Drug Administration before they can be lawfully marketed. 21......
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United States v. 14 CASES, ETC.,(BAG)" NAREMCO MEDI-MATIC
...to animal drugs. S.Rep. No. 1308, 9th Cong., 2d Sess. ___, 1968 U.S.Code, Cong. & Ad.News, pp. 2607-2613. See Agri-Tech, Inc. v. Richardson, 482 F.2d 1148, 1150 (8th Cir. 1973). 16 412 U.S. 609, 93 S.Ct. 2469, 37 L.Ed.2d 207 17 412 U.S. 645, 93 S.Ct. 2488, 37 L.Ed.2d 235 (1973). 18 412 U.S.......
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