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Canada-QC-CHICOUTIMI Azienda Directories
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Azienda News:
- Complete List of Licensed Products and Establishments | FDA
On Oct 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency We are in the process of updating FDA gov content to reflect these changes
- Drug Establishments Current Registration Site | FDA
The drug establishments current registration site is a publication of currently registered establishments which manufacture, prepare, propagate, compound or process drugs that are distributed in
- Registration and Listing | FDA - U. S. Food and Drug Administration
Domestic and foreign establishments that manufacture, repack, or re-label animal drug products in the United States are required to register with the FDA Domestic and foreign drug manufacturers
- Drug Approvals and Databases | FDA
CDER highlights key Web sites Web page provides quick links to everything from acronyms to wholesale distributor and third-party logistics providers reporting Additional topics include: approved
- Novel Drug Approvals for 2024 | FDA - U. S. Food and Drug Administration
See Drugs@FDA for information about all of CDER’s approved drugs and biological products FDA Novel Drug Therapy Approvals for 2024 The table below is a running list of CDER’s novel drugs
- FDA List of Authorized Generic Drugs | FDA - U. S. Food and Drug . . .
Subsection 505(t)(3) defines an “authorized generic drug” as a listed drug as defined in § 314 3 that has been approved under subsection 505(c) of the act and is marketed, sold, or
- Drugs@FDA - Food and Drug Administration
The majority of patient information, labels, approval letters, reviews, and other information are available for drug products approved since 1998 About Drugs@FDA Drugs@FDA allows you to search for official information about FDA approved innovator (brand name) and generic drugs and therapeutic biological products
- FDA Label Search-Company Name - Food and Drug Administration
10903 New Hampshire Avenue Silver Spring, MD 20993 Ph 1-888-INFO-FDA (1-888-463-6332) Contact FDA
- Foreign Pharmaceutical Manufacturers (5 96) | FDA
However, some compliance programs, such as the drug pre-approval and post-approval programs, may require sample collection as part of the inspection process Be guided by the respective compliance
- FDA Label Search
The drug labels and other drug-specific information on this Web site represent the most recent drug listing information companies have submitted to the Food and Drug Administration (FDA) (See 21 CFR part 207 ) The drug labeling and other information has been reformatted to make it easier to read but its content has neither been altered nor
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