busulfan
Generic: busulfan
Labeler: pharmascience inc.Drug Facts
Product Profile
Brand Name
busulfan
Generic Name
busulfan
Labeler
pharmascience inc.
Dosage Form
INJECTION
Routes
Active Ingredients
busulfan 6 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51817-170
Product ID
51817-170_df501797-3c7e-5ae2-e053-2995a90a99e8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207050
Listing Expiration
2026-12-31
Marketing Start
2017-05-19
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51817170
Hyphenated Format
51817-170
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
busulfan (source: ndc)
Generic Name
busulfan (source: ndc)
Application Number
ANDA207050 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 mg/mL
Packaging
- 8 VIAL in 1 PACKAGE (51817-170-01) / 10 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": "df501797-3c7e-5ae2-e053-2995a90a99e8", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["G1LN9045DK"], "rxcui": ["253113"], "spl_set_id": ["d0fe44f9-7747-4909-b927-3b24aa6e7e09"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Pharmascience Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 VIAL in 1 PACKAGE (51817-170-01) / 10 mL in 1 VIAL", "package_ndc": "51817-170-01", "marketing_start_date": "20170519"}], "brand_name": "Busulfan", "product_id": "51817-170_df501797-3c7e-5ae2-e053-2995a90a99e8", "dosage_form": "INJECTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "51817-170", "generic_name": "busulfan", "labeler_name": "Pharmascience Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Busulfan", "active_ingredients": [{"name": "BUSULFAN", "strength": "6 mg/mL"}], "application_number": "ANDA207050", "marketing_category": "ANDA", "marketing_start_date": "20170519", "listing_expiration_date": "20261231"}