Cyclosporine
- Product NDC
- 0093-5742
- 11-digit product format
- 000935742
- Labeler code
- 0093
- Product ID
- 0093-5742_0d006301-5ba4-46a1-a767-fbaa2a94bb75
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cyclosporine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA065110
- Marketing category
- ANDA
- Marketing start
- 2015-06-01
- Marketing end
- 2023-01-31
- Substance
- CYCLOSPORINE
- Active strength
- 100 mg/1
- 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
- 0000-00-00
- 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 |
|---|
| 0093-5742-65 | 00093574265 | 30 BLISTER PACK in 1 CARTON (0093-5742-65) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (0093-5742-19) | 30 blister pack | 2015-06-01 | 2023-01-31 | No | No | Current |