dantrium
Generic: dantrolene sodium
Labeler: par health usa, llcDrug Facts
Product Profile
Brand Name
dantrium
Generic Name
dantrolene sodium
Labeler
par health usa, llc
Dosage Form
INJECTION
Routes
Active Ingredients
dantrolene sodium 20 mg/60mL
Manufacturer
Identifiers & Regulatory
Product NDC
42023-123
Product ID
42023-123_7635e0c2-de42-44ca-9446-59bc0fc41b19
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018264
Listing Expiration
2026-12-31
Marketing Start
2009-04-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42023123
Hyphenated Format
42023-123
Supplemental Identifiers
RxCUI
UNII
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
dantrium (source: ndc)
Generic Name
dantrolene sodium (source: ndc)
Application Number
NDA018264 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/60mL
Packaging
- 6 VIAL in 1 CARTON (42023-123-06) / 60 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": "7635e0c2-de42-44ca-9446-59bc0fc41b19", "openfda": {"unii": ["287M0347EV"], "rxcui": ["856696", "856698"], "spl_set_id": ["4df35098-8702-46be-ac67-30cfdf1aa570"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 VIAL in 1 CARTON (42023-123-06) / 60 mL in 1 VIAL", "package_ndc": "42023-123-06", "marketing_start_date": "20090420"}], "brand_name": "Dantrium", "product_id": "42023-123_7635e0c2-de42-44ca-9446-59bc0fc41b19", "dosage_form": "INJECTION", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "42023-123", "generic_name": "dantrolene sodium", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dantrium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "20 mg/60mL"}], "application_number": "NDA018264", "marketing_category": "NDA", "marketing_start_date": "20090420", "listing_expiration_date": "20261231"}