procysbi
Generic: cysteamine bitartrate
Labeler: horizon therapeutics usa, inc.Drug Facts
Product Profile
Brand Name
procysbi
Generic Name
cysteamine bitartrate
Labeler
horizon therapeutics usa, inc.
Dosage Form
CAPSULE, DELAYED RELEASE PELLETS
Routes
Active Ingredients
cysteamine bitartrate 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
75987-100
Product ID
75987-100_374233b1-345c-4d9e-9bc0-e5aa2f9d8e1f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA203389
Listing Expiration
2026-12-31
Marketing Start
2013-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
75987100
Hyphenated Format
75987-100
Supplemental Identifiers
RxCUI
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
procysbi (source: ndc)
Generic Name
cysteamine bitartrate (source: ndc)
Application Number
NDA203389 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (75987-100-04)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "374233b1-345c-4d9e-9bc0-e5aa2f9d8e1f", "openfda": {"unii": ["QO84GZ3TST"], "rxcui": ["1421467", "1421473", "1421475", "1421477", "2284510", "2284514", "2284515", "2284516"], "spl_set_id": ["d3a3ec28-f746-463a-bb92-3bc8826db09e"], "manufacturer_name": ["Horizon Therapeutics USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (75987-100-04)", "package_ndc": "75987-100-04", "marketing_start_date": "20130430"}], "brand_name": "PROCYSBI", "product_id": "75987-100_374233b1-345c-4d9e-9bc0-e5aa2f9d8e1f", "dosage_form": "CAPSULE, DELAYED RELEASE PELLETS", "pharm_class": ["Cystine Depleting Agent [EPC]", "Cystine Disulfide Reduction [MoA]"], "product_ndc": "75987-100", "generic_name": "Cysteamine bitartrate", "labeler_name": "Horizon Therapeutics USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCYSBI", "active_ingredients": [{"name": "CYSTEAMINE BITARTRATE", "strength": "25 mg/1"}], "application_number": "NDA203389", "marketing_category": "NDA", "marketing_start_date": "20130430", "listing_expiration_date": "20261231"}