fingolimod
Generic: fingolimod
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
fingolimod
Generic Name
fingolimod
Labeler
sun pharmaceutical industries, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
fingolimod hydrochloride .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62756-064
Product ID
62756-064_a0abec7c-e7a2-4bbf-936a-370e0eff4e9f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208014
Listing Expiration
2026-12-31
Marketing Start
2022-10-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62756064
Hyphenated Format
62756-064
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
fingolimod (source: ndc)
Generic Name
fingolimod (source: ndc)
Application Number
ANDA208014 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 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
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a0abec7c-e7a2-4bbf-936a-370e0eff4e9f", "openfda": {"upc": ["0362756064836"], "unii": ["G926EC510T"], "rxcui": ["1012895"], "spl_set_id": ["b228dac8-b07d-424d-b23b-a03573517c54"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (62756-064-59) / 7 CAPSULE in 1 BLISTER PACK", "package_ndc": "62756-064-59", "marketing_start_date": "20221025"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (62756-064-81)", "package_ndc": "62756-064-81", "marketing_start_date": "20221025"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (62756-064-83)", "package_ndc": "62756-064-83", "marketing_start_date": "20221025"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (62756-064-96) / 14 CAPSULE in 1 BLISTER PACK", "package_ndc": "62756-064-96", "marketing_start_date": "20221025"}], "brand_name": "Fingolimod", "product_id": "62756-064_a0abec7c-e7a2-4bbf-936a-370e0eff4e9f", "dosage_form": "CAPSULE", "pharm_class": ["Sphingosine 1-Phosphate Receptor Modulators [MoA]", "Sphingosine 1-phosphate Receptor Modulator [EPC]"], "product_ndc": "62756-064", "generic_name": "Fingolimod", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fingolimod", "active_ingredients": [{"name": "FINGOLIMOD HYDROCHLORIDE", "strength": ".5 mg/1"}], "application_number": "ANDA208014", "marketing_category": "ANDA", "marketing_start_date": "20221025", "listing_expiration_date": "20261231"}