hydroxyurea
Generic: hydroxyurea
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
hydroxyurea
Generic Name
hydroxyurea
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
hydroxyurea 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-6939
Product ID
0904-6939_554e6427-7d26-4f99-b69b-10468b9bb014
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
09046939
Hyphenated Format
0904-6939
Supplemental Identifiers
RxCUI
UNII
NUI
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 BLISTER PACK in 1 CARTON (0904-6939-61) / 1 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "554e6427-7d26-4f99-b69b-10468b9bb014", "openfda": {"nui": ["N0000180853", "M0022315"], "unii": ["X6Q56QN5QC"], "rxcui": ["197797"], "spl_set_id": ["e76fd60e-7644-48c5-9857-3608a045000b"], "pharm_class_cs": ["Urea [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6939-61) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-6939-61", "marketing_start_date": "19990224"}], "brand_name": "Hydroxyurea", "product_id": "0904-6939_554e6427-7d26-4f99-b69b-10468b9bb014", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite [EPC]", "Urea [CS]"], "product_ndc": "0904-6939", "generic_name": "Hydroxyurea", "labeler_name": "Major Pharmaceuticals", "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"}