NDC 67877-476 – Fingolimod

Fingolimod Hydrochloride .5 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

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

Uses, dosage, side effects and warnings for Fingolimod →

Package NDC codes (5)

Package NDCDescriptionSince
67877-476-3030 CAPSULE in 1 BOTTLE (67877-476-30)Sep 21, 2022
67877-476-327 BLISTER PACK in 1 CARTON (67877-476-32) / 7 CAPSULE in 1 BLISTER PACKSep 21, 2022
67877-476-3310 BLISTER PACK in 1 CARTON (67877-476-33) / 10 CAPSULE in 1 BLISTER PACKSep 21, 2022
67877-476-5628 CAPSULE in 1 BOTTLE (67877-476-56)Sep 21, 2022
67877-476-5828 BLISTER PACK in 1 CARTON (67877-476-58) / 14 CAPSULE in 1 BLISTER PACK (67877-476-14)Sep 21, 2022

Recalls mentioning this NDC

Other Fingolimod products