nelarabine
Generic: nelarabine
Labeler: meitheal pharmaceuticals incDrug Facts
Product Profile
Brand Name
nelarabine
Generic Name
nelarabine
Labeler
meitheal pharmaceuticals inc
Dosage Form
INJECTION
Routes
Active Ingredients
nelarabine 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-165
Product ID
71288-165_6e728854-7685-4806-8edb-e2a3fc055c7d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216038
Listing Expiration
2026-12-31
Marketing Start
2023-01-10
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288165
Hyphenated Format
71288-165
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
nelarabine (source: ndc)
Generic Name
nelarabine (source: ndc)
Application Number
ANDA216038 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-165-54) / 50 mL in 1 VIAL, SINGLE-DOSE (71288-165-52)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6e728854-7685-4806-8edb-e2a3fc055c7d", "openfda": {"nui": ["N0000000233", "N0000175595"], "unii": ["60158CV180"], "rxcui": ["603566"], "spl_set_id": ["21919314-5c25-49ab-beba-099983ed4a71"], "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 (71288-165-54) / 50 mL in 1 VIAL, SINGLE-DOSE (71288-165-52)", "package_ndc": "71288-165-54", "marketing_start_date": "20230110"}], "brand_name": "Nelarabine", "product_id": "71288-165_6e728854-7685-4806-8edb-e2a3fc055c7d", "dosage_form": "INJECTION", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleoside Metabolic Inhibitor [EPC]"], "product_ndc": "71288-165", "generic_name": "Nelarabine", "labeler_name": "Meitheal Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nelarabine", "active_ingredients": [{"name": "NELARABINE", "strength": "5 mg/mL"}], "application_number": "ANDA216038", "marketing_category": "ANDA", "marketing_start_date": "20230110", "listing_expiration_date": "20261231"}