decitabine
Generic: decitabine
Labeler: qilu pharmaceutical co., ltd.Drug Facts
Product Profile
Brand Name
decitabine
Generic Name
decitabine
Labeler
qilu pharmaceutical co., ltd.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
decitabine 50 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
67184-0535
Product ID
67184-0535_0afb3dc7-6072-4a53-acc4-59589fb8491e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212826
Listing Expiration
2026-12-31
Marketing Start
2021-04-12
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
671840535
Hyphenated Format
67184-0535
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
decitabine (source: ndc)
Generic Name
decitabine (source: ndc)
Application Number
ANDA212826 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/20mL
Packaging
- 1 VIAL in 1 CARTON (67184-0535-1) / 20 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0afb3dc7-6072-4a53-acc4-59589fb8491e", "openfda": {"nui": ["N0000000233", "N0000175595"], "upc": ["0367184053513"], "unii": ["776B62CQ27"], "rxcui": ["636631"], "spl_set_id": ["5b2dce6f-c715-47dc-971e-06244ccd7548"], "pharm_class_epc": ["Nucleoside Metabolic Inhibitor [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (67184-0535-1) / 20 mL in 1 VIAL", "package_ndc": "67184-0535-1", "marketing_start_date": "20210412"}], "brand_name": "Decitabine", "product_id": "67184-0535_0afb3dc7-6072-4a53-acc4-59589fb8491e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "67184-0535", "generic_name": "decitabine", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Decitabine", "active_ingredients": [{"name": "DECITABINE", "strength": "50 mg/20mL"}], "application_number": "ANDA212826", "marketing_category": "ANDA", "marketing_start_date": "20210412", "listing_expiration_date": "20261231"}