WILPO
PHENTERMINE HYDROCHLORIDE
Approval overview WILPO is listed in Drugs@FDA under application 012737 (NDA).
Marketing status: Discontinued Active ingredient PHENTERMINE HYDROCHLORIDE Form and strength TABLET;ORAL - 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANDOZ Submission history See approval history documents.
Structured Monograph
Clinical summary
Approval overview WILPO is listed in Drugs@FDA under application 012737 (NDA). Marketing status: Discontinued Active ingredient PHENTERMINE HYDROCHLORIDE Form and strength TABLET;ORAL - 8MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANDOZ Submission history See approval history documents.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.