AMPHETAMINE SULFATE (AMPHETAMINE SULFATE) — FDA Approval ANDA213898 (DR REDDYS LABS SA)
AMPHETAMINE SULFATE (AMPHETAMINE SULFATE) — FDA Approval ANDA213898 (DR REDDYS LABS SA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: AMPHETAMINE SULFATE; Active ingredients: AMPHETAMINE SULFATE; Application number: ANDA213898.
| Brand name | AMPHETAMINE SULFATE |
|---|---|
| Active ingredients | AMPHETAMINE SULFATE |
| Application number | ANDA213898 |
| Sponsor | DR REDDYS LABS SA |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 20200714 |
| Source | openFDA Drugs@FDA |
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