dacarbazine
Generic: dacarbazine
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
dacarbazine
Generic Name
dacarbazine
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
dacarbazine 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9245
Product ID
0143-9245_bbbf119e-26f4-46c1-ba80-de927e51c566
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075812
Listing Expiration
2026-12-31
Marketing Start
2001-08-08
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439245
Hyphenated Format
0143-9245
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
dacarbazine (source: ndc)
Generic Name
dacarbazine (source: ndc)
Application Number
ANDA075812 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 10 VIAL in 1 CARTON (0143-9245-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9245-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "bbbf119e-26f4-46c1-ba80-de927e51c566", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["7GR28W0FJI"], "rxcui": ["1731338"], "spl_set_id": ["0d81315c-7021-4091-b703-ad135390c936"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (0143-9245-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (0143-9245-01)", "package_ndc": "0143-9245-10", "marketing_start_date": "20010808"}], "brand_name": "Dacarbazine", "product_id": "0143-9245_bbbf119e-26f4-46c1-ba80-de927e51c566", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "0143-9245", "generic_name": "Dacarbazine", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dacarbazine", "active_ingredients": [{"name": "DACARBAZINE", "strength": "200 mg/1"}], "application_number": "ANDA075812", "marketing_category": "ANDA", "marketing_start_date": "20010808", "listing_expiration_date": "20261231"}