Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 074555
Company: TEVA PHARMS
Company: TEVA PHARMS
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| CHOLESTYRAMINE LIGHT | CHOLESTYRAMINE | EQ 4GM RESIN/PACKET | POWDER;ORAL | Discontinued | None | No | No |
| CHOLESTYRAMINE LIGHT | CHOLESTYRAMINE | EQ 4GM RESIN/SCOOPFUL | POWDER;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 |
|---|---|---|---|---|---|---|---|
| 09/30/1998 | ORIG-1 | Approval |
Letter (PDF)
Review (PDF) |
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/1998/74555LTR.PDF https://www.accessdata.fda.gov/drugsatfda_docs/anda/98/74555_Cholestramine.pdf |