Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 010679
Company: SANOFI AVENTIS US
Company: SANOFI AVENTIS US
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
CANTIL | MEPENZOLATE BROMIDE | 25MG | TABLET;ORAL | Discontinued | None | Yes | No |
CANTIL | MEPENZOLATE BROMIDE | 25MG/5ML | SOLUTION;ORAL | Discontinued | None | No | No |
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert |
Note | Url |
---|---|---|---|---|---|
05/25/2004 | SUPPL-29 | Labeling | Label (PDF) | https://www.accessdata.fda.gov/drugsatfda_docs/label/2004/10679slr029_cantil_lbl.pdf |