anagrelide
Generic: anagrelide
Labeler: torrent pharmaceuticals limitedDrug Facts
Product Profile
Brand Name
anagrelide
Generic Name
anagrelide
Labeler
torrent pharmaceuticals limited
Dosage Form
CAPSULE
Routes
Active Ingredients
anagrelide hydrochloride anhydrous 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
13668-462
Product ID
13668-462_a049d02a-22e1-4ea2-8c05-50b50cef4362
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209151
Listing Expiration
2026-12-31
Marketing Start
2017-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
13668462
Hyphenated Format
13668-462
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
ANDA209151 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (13668-462-01)
- 30 CAPSULE in 1 BOTTLE (13668-462-30)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a049d02a-22e1-4ea2-8c05-50b50cef4362", "openfda": {"upc": ["0313668453300", "0313668462302"], "unii": ["VNS4435G39"], "rxcui": ["597850", "597852"], "spl_set_id": ["875cc32a-219c-4b6b-802a-98a47cbc9a78"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (13668-462-01)", "package_ndc": "13668-462-01", "marketing_start_date": "20170630"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (13668-462-30)", "package_ndc": "13668-462-30", "marketing_start_date": "20170630"}], "brand_name": "anagrelide", "product_id": "13668-462_a049d02a-22e1-4ea2-8c05-50b50cef4362", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Platelet Production [PE]", "Phosphodiesterase 3 Inhibitors [MoA]", "Platelet-reducing Agent [EPC]"], "product_ndc": "13668-462", "generic_name": "anagrelide", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "anagrelide", "active_ingredients": [{"name": "ANAGRELIDE HYDROCHLORIDE ANHYDROUS", "strength": "1 mg/1"}], "application_number": "ANDA209151", "marketing_category": "ANDA", "marketing_start_date": "20170630", "listing_expiration_date": "20261231"}