legislation: 106-hr-5313
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| bill_id | congress | bill_type | bill_number | title | policy_area | introduced_date | latest_action_date | latest_action_text | origin_chamber | sponsor_name | sponsor_state | sponsor_party | sponsor_bioguide_id | cosponsor_count | summary_text | update_date | url |
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| 106-hr-5313 | 106 | hr | 5313 | Drug Competition Act of 2000 | Commerce | 2000-09-27 | 2000-10-20 | Referred to the Subcommittee on Health and Environment. | House | Rep. Andrews, Robert E. [D-NJ-1] | NJ | D | A000210 | 0 | Drug Competition Act of 2000 - Requires brand name drug manufacturers and generic drug manufacturers to notify the Federal Trade Commission and the Attorney General of agreements regarding the sale or manufacture of generic drugs which could have the effect of limiting the research, development, manufacture, marketing, or selling of a generic drug product. | 2025-08-20T14:20:48Z |