Fingolimod 62756-0064
Product NDC
62756-0064- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 25, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA208014
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fingolimod Hydrochloride | .5 mg/1 |
Drug Class
Sphingosine 1-Phosphate Receptor Modulators [MoA]Sphingosine 1-phosphate Receptor Modulator [EPC]
Packaging Options(4)
1 BLISTER PACK in 1 CARTON (62756-064-59) / 7 CAPSULE in 1 BLISTER PACK
90 CAPSULE in 1 BOTTLE (62756-064-81)
30 CAPSULE in 1 BOTTLE (62756-064-83)
2 BLISTER PACK in 1 CARTON (62756-064-96) / 14 CAPSULE in 1 BLISTER PACK