ACARBOSE | A077532 | WATSON LABORATORIES INC
| Petition | Type | Filed | Status | Petitioner |
|---|---|---|---|---|
Cobalt Laboratories, Inc. and Cobalt Pharmaceuticals, Inc. - Citizen Petition FDA-2007-P-0418 · 5 docket documents Cobalt Laboratories Inc. and Cobalt Pharmaceuticals Inc. filed this citizen petition on November 9, 2007, requesting that the FDA require all ANDA applicants referencing Bayer's NDA No. 20-482 for Precose (acarbose) to conduct in vivo bioequivalence studies and refrain from granting any bioequivalen | 505(q) | 2008-04-22 | Denied | — |
Source: Regulations.gov. FDA citizen petitions matched by application number.
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