Details for New Drug Application (NDA): 019972
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The generic ingredient in OCUPRESS is carteolol hydrochloride. There are four drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the carteolol hydrochloride profile page.
Summary for 019972
| Tradename: | OCUPRESS |
| Applicant: | Novartis |
| Ingredient: | carteolol hydrochloride |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 019972
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | SOLUTION/DROPS;OPHTHALMIC | Strength | 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | ||||
| Approval Date: | May 23, 1990 | TE: | RLD: | Yes | |||||
Expired US Patents for NDA 019972
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
|---|---|---|---|---|---|---|---|
| Novartis | OCUPRESS | carteolol hydrochloride | SOLUTION/DROPS;OPHTHALMIC | 019972-001 | May 23, 1990 | ⤷ Start Trial | ⤷ Start Trial |
| Novartis | OCUPRESS | carteolol hydrochloride | SOLUTION/DROPS;OPHTHALMIC | 019972-001 | May 23, 1990 | ⤷ Start Trial | ⤷ Start Trial |
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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