Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 204119
Company: HETERO DRUGS LTD
Company: HETERO DRUGS LTD
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| EFAVIRENZ, LAMIVUDINE, AND TENOFOVIR DISOPROXIL FUMARATE | EFAVIRENZ;LAMIVUDINE;TENOFOVIR DISOPROXIL FUMARATE | 600MG;300MG;300MG | TABLET; ORAL | None (Tentative Approval) | 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 |
|---|---|---|---|---|---|---|---|
| 06/30/2017 | ORIG-1 | Tentative Approval | Type 4 - New Combination | PRIORITY |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2012/204119Orig1s000TAltr.pdf |