Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 073462
Company: CHARTWELL RX
Company: CHARTWELL RX
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
TOLMETIN SODIUM | TOLMETIN SODIUM | EQ 400MG BASE | CAPSULE;ORAL | Discontinued | None | No | 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 |
---|---|---|---|---|---|---|---|
04/30/1992 | ORIG-1 | Approval |
Label is not available on this site. |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
04/28/2021 | SUPPL-6 | Labeling-Package Insert |
Label is not available on this site. |
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04/05/2021 | SUPPL-5 | Labeling-Medication Guide, Labeling-Package Insert |
Label is not available on this site. |
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05/09/2016 | SUPPL-4 | Labeling-Patient Package Insert, Labeling-Package Insert |
Label is not available on this site. |
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05/09/2001 | SUPPL-3 | Manufacturing (CMC)-Control |
Label is not available on this site. |
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04/14/2001 | SUPPL-2 | Manufacturing (CMC)-Control |
Label is not available on this site. |
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01/24/1994 | SUPPL-1 | Manufacturing (CMC) |
Label is not available on this site. |