Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 012594
Company: SANOFI AVENTIS US
Company: SANOFI AVENTIS US
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
METAHYDRIN | TRICHLORMETHIAZIDE | 2MG | TABLET;ORAL | Discontinued | None | No | No |
METAHYDRIN | TRICHLORMETHIAZIDE | 4MG | TABLET;ORAL | Discontinued | None | No | No |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
01/28/1994 | SUPPL-18 | Labeling |
Label is not available on this site. |
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06/23/1989 | SUPPL-17 | Labeling |
Label is not available on this site. |
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06/16/1988 | SUPPL-16 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
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06/16/1988 | SUPPL-15 | Manufacturing (CMC) |
Label is not available on this site. |
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06/16/1988 | SUPPL-13 | Labeling |
Label is not available on this site. |
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06/16/1988 | SUPPL-8 | Manufacturing (CMC)-Control |
Label is not available on this site. |