Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 213763
Company: NOVAST LABS
Company: NOVAST LABS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
AMPHETAMINE SULFATE | AMPHETAMINE SULFATE | 5MG | TABLET;ORAL | Discontinued | None | No | No |
AMPHETAMINE SULFATE | AMPHETAMINE SULFATE | 10MG | 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 |
---|---|---|---|---|---|---|---|
08/24/2020 | ORIG-1 | Approval | STANDARD |
Label is not available on this site. |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
10/13/2023 | SUPPL-2 | Labeling-Package Insert |
Label is not available on this site. |
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02/25/2022 | SUPPL-1 | Labeling-Package Insert |
Label is not available on this site. |