NDC 67877-476 – Fingolimod
Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral
Product NDC67877-476
Product details
- Brand name
- Fingolimod
- Generic name
- Fingolimod hydrochloride
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA208004
- Marketed since
- September 21, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Sphingosine 1-phosphate Receptor Modulator
Active ingredients
- Fingolimod Hydrochloride .5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 67877-476-30 | 30 CAPSULE in 1 BOTTLE (67877-476-30) | Sep 21, 2022 |
| 67877-476-32 | 7 BLISTER PACK in 1 CARTON (67877-476-32) / 7 CAPSULE in 1 BLISTER PACK | Sep 21, 2022 |
| 67877-476-33 | 10 BLISTER PACK in 1 CARTON (67877-476-33) / 10 CAPSULE in 1 BLISTER PACK | Sep 21, 2022 |
| 67877-476-56 | 28 CAPSULE in 1 BOTTLE (67877-476-56) | Sep 21, 2022 |
| 67877-476-58 | 28 BLISTER PACK in 1 CARTON (67877-476-58) / 14 CAPSULE in 1 BLISTER PACK (67877-476-14) | Sep 21, 2022 |
Recalls mentioning this NDC
- D-0925-2023 Jul 26, 2023 · Class II
Failed Dissolution Specifications
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