Rulemaking History for OTC Cholecystokinetic Drug Products View by Topic
Final Monograph (21 CFR part 357 subpart C):
Miscellaneous Internal Drug Products for Over-the-Counter Human Use:
Cholecystokinetic Drug Products
|
Date |
Federal Register Citation |
Description |
2/12/1980 |
45FR9286
![PDF document](https://webarchive.library.unt.edu/eot2008/20081106191632im_/http://www.fda.gov/cder/graphics/pdf.gif) |
Advance
Notice of Proposed Rulemaking |
8/24/1982 |
47FR37068
![PDF document](https://webarchive.library.unt.edu/eot2008/20081106191632im_/http://www.fda.gov/cder/graphics/pdf.gif) |
Tentative Final Monograph |
6/10/1983 |
48FR27004
![PDF document](https://webarchive.library.unt.edu/eot2008/20081106191632im_/http://www.fda.gov/cder/graphics/pdf.gif) |
Final Monograph |
8/15/1988 |
53FR30786
![PDF document](https://webarchive.library.unt.edu/eot2008/20081106191632im_/http://www.fda.gov/cder/graphics/pdf.gif) |
Proposed
Rule: Adds hydrogenated soybean oil as GRASE
active ingredient |
2/28/1989 |
54FR8320
![PDF document](https://webarchive.library.unt.edu/eot2008/20081106191632im_/http://www.fda.gov/cder/graphics/pdf.gif) |
Final
Rule: Adds hydrogenated soybean oil as GRASE
active ingredient |
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Date updated: May 9, 2007 |