agrylin
Generic: anagrelide hydrochloride
Labeler: takeda pharmaceuticals america, inc.Drug Facts
Product Profile
Brand Name
agrylin
Generic Name
anagrelide hydrochloride
Labeler
takeda pharmaceuticals america, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
anagrelide hydrochloride anhydrous .5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
54092-063
Product ID
54092-063_06f9dfa4-c90a-4636-b3b1-79b488815bb3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020333
Listing Expiration
2026-12-31
Marketing Start
1997-03-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
54092063
Hyphenated Format
54092-063
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
agrylin (source: ndc)
Generic Name
anagrelide hydrochloride (source: ndc)
Application Number
NDA020333 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (54092-063-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06f9dfa4-c90a-4636-b3b1-79b488815bb3", "openfda": {"upc": ["0354092063017"], "unii": ["VNS4435G39"], "rxcui": ["597850", "597857"], "spl_set_id": ["cb960074-99c1-4a73-941f-f0644a7ec219"], "manufacturer_name": ["Takeda Pharmaceuticals America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (54092-063-01)", "package_ndc": "54092-063-01", "marketing_start_date": "19970314"}], "brand_name": "Agrylin", "product_id": "54092-063_06f9dfa4-c90a-4636-b3b1-79b488815bb3", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Platelet Production [PE]", "Phosphodiesterase 3 Inhibitors [MoA]", "Platelet-reducing Agent [EPC]"], "product_ndc": "54092-063", "generic_name": "anagrelide hydrochloride", "labeler_name": "Takeda Pharmaceuticals America, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Agrylin", "active_ingredients": [{"name": "ANAGRELIDE HYDROCHLORIDE ANHYDROUS", "strength": ".5 mg/1"}], "application_number": "NDA020333", "marketing_category": "NDA", "marketing_start_date": "19970314", "listing_expiration_date": "20261231"}