decitabine
Generic: decitabine
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
decitabine
Generic Name
decitabine
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
decitabine 50 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-119
Product ID
71288-119_b607f279-446f-43d6-b0ef-1d8e48366c87
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212959
Listing Expiration
2026-12-31
Marketing Start
2021-07-02
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288119
Hyphenated Format
71288-119
Supplemental Identifiers
RxCUI
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
ANDA212959 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/20mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-119-20) / 20 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b607f279-446f-43d6-b0ef-1d8e48366c87", "openfda": {"nui": ["N0000000233", "N0000175595"], "unii": ["776B62CQ27"], "rxcui": ["636631"], "spl_set_id": ["a535a235-e1d2-4520-93fe-b7dd9b047784"], "pharm_class_epc": ["Nucleoside Metabolic Inhibitor [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-119-20) / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-119-20", "marketing_start_date": "20210702"}], "brand_name": "Decitabine", "product_id": "71288-119_b607f279-446f-43d6-b0ef-1d8e48366c87", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "71288-119", "generic_name": "Decitabine", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Decitabine", "active_ingredients": [{"name": "DECITABINE", "strength": "50 mg/20mL"}], "application_number": "ANDA212959", "marketing_category": "ANDA", "marketing_start_date": "20210702", "listing_expiration_date": "20261231"}