anagrelide
Generic: anagrelide
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
anagrelide
Generic Name
anagrelide
Labeler
chartwell rx, llc
Dosage Form
CAPSULE
Routes
Active Ingredients
anagrelide hydrochloride anhydrous 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-313
Product ID
62135-313_13156e50-28d1-0994-e063-6394a90a16ec
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076683
Listing Expiration
2026-12-31
Marketing Start
2005-04-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135313
Hyphenated Format
62135-313
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
anagrelide (source: ndc)
Generic Name
anagrelide (source: ndc)
Application Number
ANDA076683 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 60 CAPSULE in 1 BOTTLE (62135-313-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "13156e50-28d1-0994-e063-6394a90a16ec", "openfda": {"upc": ["0362135312121", "0362135313609"], "unii": ["VNS4435G39"], "rxcui": ["597850", "597852"], "spl_set_id": ["e031dfb3-56e1-4fea-95f2-c2936e2057a0"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (62135-313-60)", "package_ndc": "62135-313-60", "marketing_start_date": "20240205"}], "brand_name": "Anagrelide", "product_id": "62135-313_13156e50-28d1-0994-e063-6394a90a16ec", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Platelet Production [PE]", "Phosphodiesterase 3 Inhibitors [MoA]", "Platelet-reducing Agent [EPC]"], "product_ndc": "62135-313", "generic_name": "Anagrelide", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anagrelide", "active_ingredients": [{"name": "ANAGRELIDE HYDROCHLORIDE ANHYDROUS", "strength": "1 mg/1"}], "application_number": "ANDA076683", "marketing_category": "ANDA", "marketing_start_date": "20050418", "listing_expiration_date": "20261231"}