decitabine
Generic: decitabine
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
decitabine
Generic Name
decitabine
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
decitabine 50 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-825
Product ID
63323-825_d3d820f1-175e-4613-bdab-74c15f45912e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210756
Listing Expiration
2026-12-31
Marketing Start
2019-12-02
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323825
Hyphenated Format
63323-825
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
ANDA210756 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/20mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-825-20) / 20 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d3d820f1-175e-4613-bdab-74c15f45912e", "openfda": {"nui": ["N0000000233", "N0000175595"], "unii": ["776B62CQ27"], "rxcui": ["636631"], "spl_set_id": ["4d568777-0946-489c-99bf-57e1f562e285"], "pharm_class_epc": ["Nucleoside Metabolic Inhibitor [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (63323-825-20) / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "63323-825-20", "marketing_start_date": "20191202"}], "brand_name": "Decitabine", "product_id": "63323-825_d3d820f1-175e-4613-bdab-74c15f45912e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "63323-825", "generic_name": "Decitabine", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Decitabine", "active_ingredients": [{"name": "DECITABINE", "strength": "50 mg/20mL"}], "application_number": "ANDA210756", "marketing_category": "ANDA", "marketing_start_date": "20191202", "listing_expiration_date": "20261231"}