hydroxyurea
Generic: hydroxyurea
Labeler: endo usa, inc.Drug Facts
Product Profile
Brand Name
hydroxyurea
Generic Name
hydroxyurea
Labeler
endo usa, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
hydroxyurea 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
49884-724
Product ID
49884-724_a413e3e0-7f61-4b1a-af2c-dae9e63a3972
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075340
Listing Expiration
2026-12-31
Marketing Start
1999-02-24
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
49884724
Hyphenated Format
49884-724
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
hydroxyurea (source: ndc)
Generic Name
hydroxyurea (source: ndc)
Application Number
ANDA075340 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (49884-724-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a413e3e0-7f61-4b1a-af2c-dae9e63a3972", "openfda": {"nui": ["N0000180853", "M0022315"], "upc": ["0349884724016"], "unii": ["X6Q56QN5QC"], "rxcui": ["197797"], "spl_set_id": ["9e1bdd4b-043a-4cf6-b1ff-8de49e02b7a6"], "pharm_class_cs": ["Urea [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (49884-724-01)", "package_ndc": "49884-724-01", "marketing_start_date": "19990224"}], "brand_name": "Hydroxyurea", "product_id": "49884-724_a413e3e0-7f61-4b1a-af2c-dae9e63a3972", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite [EPC]", "Urea [CS]"], "product_ndc": "49884-724", "generic_name": "Hydroxyurea", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyurea", "active_ingredients": [{"name": "HYDROXYUREA", "strength": "500 mg/1"}], "application_number": "ANDA075340", "marketing_category": "ANDA", "marketing_start_date": "19990224", "listing_expiration_date": "20261231"}