Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 089162
Company: ALCON PHARMS LTD
Company: ALCON PHARMS LTD
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| CYCLOPENTOLATE HYDROCHLORIDE | CYCLOPENTOLATE HYDROCHLORIDE | 1% | SOLUTION/DROPS;OPHTHALMIC | 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 |
|---|---|---|---|---|---|---|---|
| 01/24/1991 | 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 |
|---|---|---|---|---|---|
| 06/07/1996 | SUPPL-4 | Manufacturing (CMC) |
Label is not available on this site. |
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| 06/07/1996 | SUPPL-3 | Manufacturing (CMC) |
Label is not available on this site. |
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| 04/16/1996 | SUPPL-2 | Manufacturing (CMC) |
Label is not available on this site. |
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| 06/20/1994 | SUPPL-1 | Labeling |
Label is not available on this site. |