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dockets: FDA-2003-P-0120

Regulatory dockets from Regulations.gov — containers for related documents and comments in a rulemaking proceeding.

This data as json

id agency_id title docket_type last_modified object_id
FDA-2003-P-0120 FDA Request whether Cataflam (diclofenac Potassium) Tablets 25 mg (NDA 20-12) mfged by Novartis Pharmaceuticals Corporation, has been voluntarily withdrawn or withheld from sale for safety or effectiveness reasons. Nonrulemaking 2021-09-01T01:02:56Z 0b0000648048599d

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  • 2 rows from docket_id in documents
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