dacarbazine
Generic: dacarbazine
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
dacarbazine
Generic Name
dacarbazine
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
dacarbazine 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-127
Product ID
63323-127_04644165-06c9-4a55-a026-a529d824cc90
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075371
Listing Expiration
2026-12-31
Marketing Start
2001-09-07
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323127
Hyphenated Format
63323-127
Supplemental Identifiers
RxCUI
UPC
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
ANDA075371 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 TRAY (63323-127-10) / 10 mL in 1 VIAL, SINGLE-DOSE (63323-127-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "04644165-06c9-4a55-a026-a529d824cc90", "openfda": {"nui": ["N0000000236", "N0000175558"], "upc": ["0363323128005", "0363323127008"], "unii": ["7GR28W0FJI"], "rxcui": ["1731338", "1731340"], "spl_set_id": ["b6b97e41-5f15-498c-abfb-d8443ea4d216"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 TRAY (63323-127-10) / 10 mL in 1 VIAL, SINGLE-DOSE (63323-127-00)", "package_ndc": "63323-127-10", "marketing_start_date": "20010907"}], "brand_name": "Dacarbazine", "product_id": "63323-127_04644165-06c9-4a55-a026-a529d824cc90", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "63323-127", "generic_name": "DACARBAZINE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dacarbazine", "active_ingredients": [{"name": "DACARBAZINE", "strength": "10 mg/mL"}], "application_number": "ANDA075371", "marketing_category": "ANDA", "marketing_start_date": "20010907", "listing_expiration_date": "20261231"}