Format & content for new OTC drug products (included FDA recommendations on statutory requirements)

General Drug Labeling Provisions and OTC Monograph Drug User Fee Submissions

FFDCA Sec 502 - 21 USC 352

Format & content for new OTC drug products (included FDA recommendations on statutory requirements)

OMB: 0910-0340

Document [html]
Download: html







The system is under maintenance. It will be back shortly.

File Typetext/html

© 2025 OMB.report | Privacy Policy