Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 070999
Company: FUTURE PAK
Company: FUTURE PAK
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
K+10 | POTASSIUM CHLORIDE | 10MEQ | TABLET, EXTENDED RELEASE;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 |
---|---|---|---|---|---|---|---|
10/22/1987 | 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 |
---|---|---|---|---|---|
06/23/1995 | SUPPL-7 | Manufacturing (CMC) |
Label is not available on this site. |
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06/23/1995 | SUPPL-6 | Manufacturing (CMC) |
Label is not available on this site. |
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07/22/1994 | SUPPL-5 | Manufacturing (CMC) |
Label is not available on this site. |
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11/16/1992 | SUPPL-4 | Bioequivalence |
Label is not available on this site. |