PHENTERMINE HYDROCHLORIDE | A203436 | KVK TECH INC
| Petition | Type | Filed | Status | Petitioner |
|---|---|---|---|---|
KVK-Tech, Inc. - Citizen Petition FDA-2011-P-0701 · 4 docket documents KVK-Tech, Inc. filed this relisting petition under 21 CFR 314.122 requesting that the FDA determine whether Wilpro Tablets (phentermine hydrochloride 8 mg), NDA 012737 originally held by Sandoz, was withdrawn from sale for reasons of safety or effectiveness, and if not, to relist the NDA to allow AN | 505(q) | 2011-10-07 | Granted | — |
Source: Regulations.gov. FDA citizen petitions matched by application number.
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