Cyclosporine
- Product NDC
- 50090-5977
- 11-digit product format
- 500905977
- Labeler code
- 50090
- Product ID
- 50090-5977_9bc080ff-be76-43c7-9fcb-96030b307c28
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclosporine
- Dosage form
- EMULSION
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- NDA050790
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2022-02-07
- Marketing end
- 0000-00-00
- Substance
- CYCLOSPORINE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Calcineurin Inhibitor Immunosuppressant [EPC], Calcineurin Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5977-0 | 50090597700 | 30 VIAL in 1 TRAY (50090-5977-0) > .4 mL in 1 VIAL | 30 vial | 2022-05-05 | 0000-00-00 | No | No | Current |