Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 073357
Company: CHARTWELL RX
Company: CHARTWELL RX
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
AMILORIDE HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE | AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE | EQ 5MG ANHYDROUS;50MG | 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 |
---|---|---|---|---|---|---|---|
11/27/1991 | 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 |
---|---|---|---|---|---|
08/20/2020 | SUPPL-9 | Labeling-Package Insert |
Label is not available on this site. |
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08/06/2020 | SUPPL-8 | Labeling-Package Insert |
Label is not available on this site. |
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12/01/1998 | SUPPL-7 | Manufacturing (CMC) |
Label is not available on this site. |
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12/01/1998 | SUPPL-6 | Manufacturing (CMC) |
Label is not available on this site. |
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06/12/1998 | SUPPL-5 | Manufacturing (CMC) |
Label is not available on this site. |
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08/27/1996 | SUPPL-4 | Manufacturing (CMC) |
Label is not available on this site. |
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08/27/1996 | SUPPL-3 | Manufacturing (CMC) |
Label is not available on this site. |
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11/15/1993 | SUPPL-2 | Labeling |
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. |