hydroxyurea
Generic: hydroxyurea
Labeler: qilu pharmaceutical co., ltd.Drug Facts
Product Profile
Brand Name
hydroxyurea
Generic Name
hydroxyurea
Labeler
qilu pharmaceutical co., ltd.
Dosage Form
CAPSULE
Routes
Active Ingredients
hydroxyurea 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67184-0607
Product ID
67184-0607_a252a0db-b5ce-49d2-b29d-461b34a41479
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218021
Listing Expiration
2026-12-31
Marketing Start
2024-03-06
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
671840607
Hyphenated Format
67184-0607
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
ANDA218021 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (67184-0607-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a252a0db-b5ce-49d2-b29d-461b34a41479", "openfda": {"nui": ["N0000180853", "M0022315"], "upc": ["0367184060719"], "unii": ["X6Q56QN5QC"], "rxcui": ["197797"], "spl_set_id": ["4cd244d4-bd4a-41c8-b072-c2135787d412"], "pharm_class_cs": ["Urea [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (67184-0607-1)", "package_ndc": "67184-0607-1", "marketing_start_date": "20240306"}], "brand_name": "HYDROXYUREA", "product_id": "67184-0607_a252a0db-b5ce-49d2-b29d-461b34a41479", "dosage_form": "CAPSULE", "pharm_class": ["Antimetabolite [EPC]", "Urea [CS]"], "product_ndc": "67184-0607", "generic_name": "HYDROXYUREA", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYUREA", "active_ingredients": [{"name": "HYDROXYUREA", "strength": "500 mg/1"}], "application_number": "ANDA218021", "marketing_category": "ANDA", "marketing_start_date": "20240306", "listing_expiration_date": "20261231"}