Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 020617
Company: AVENT
Company: AVENT
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| PYTEST | UREA, C-14 | 1uCi | CAPSULE;ORAL | Discontinued | None | Yes | No |
| PYTEST KIT | UREA, C-14 | 1uCi **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL | Discontinued | None | Yes | No |
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
|---|---|---|---|---|---|---|---|
| 05/09/1997 | ORIG-1 | Approval | Type 1 - New Molecular Entity | PRIORITY |
Label is not available on this site. |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 01/31/2014 | SUPPL-4 | Labeling-Container/Carton Labels |
Label is not available on this site. |
||
| 03/17/2000 | SUPPL-1 | Manufacturing (CMC) |
Label is not available on this site. |