Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 075663
Company: IMPAX PHARMS
Company: IMPAX PHARMS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
SOTALOL HYDROCHLORIDE | SOTALOL HYDROCHLORIDE | 80MG | TABLET;ORAL | Discontinued | None | No | No |
SOTALOL HYDROCHLORIDE | SOTALOL HYDROCHLORIDE | 120MG | TABLET;ORAL | Discontinued | None | No | No |
SOTALOL HYDROCHLORIDE | SOTALOL HYDROCHLORIDE | 160MG | TABLET;ORAL | Discontinued | None | No | No |
SOTALOL HYDROCHLORIDE | SOTALOL HYDROCHLORIDE | 240MG | TABLET;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 |
---|---|---|---|---|---|---|---|
11/07/2000 | ORIG-1 | Approval |
Letter (PDF)
Review (PDF) |
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2000/75663ltr.pdf https://www.accessdata.fda.gov/drugsatfda_docs/nda/2000/075663.PDF |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
12/06/2023 | SUPPL-6 | Labeling-Package Insert |
Label is not available on this site. |
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02/28/2023 | SUPPL-5 | Labeling-Package Insert |
Label is not available on this site. |
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02/16/2021 | SUPPL-3 | Labeling-Package Insert |
Label is not available on this site. |
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10/03/2002 | SUPPL-1 | Labeling |
Label is not available on this site. |