dantrolene sodium
Generic: dantrolene sodium
Labeler: elite laboratories, inc.Drug Facts
Product Profile
Brand Name
dantrolene sodium
Generic Name
dantrolene sodium
Labeler
elite laboratories, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
dantrolene sodium 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
64850-840
Product ID
64850-840_e3fc6ec6-cdde-456a-81bd-8ebd07065afc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076686
Listing Expiration
2026-12-31
Marketing Start
2005-10-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64850840
Hyphenated Format
64850-840
Supplemental Identifiers
RxCUI
UPC
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
dantrolene sodium (source: ndc)
Generic Name
dantrolene sodium (source: ndc)
Application Number
ANDA076686 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (64850-840-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3fc6ec6-cdde-456a-81bd-8ebd07065afc", "openfda": {"upc": ["0364850842013", "0364850840019", "0364850841016"], "unii": ["287M0347EV"], "rxcui": ["856652", "856656", "856660"], "spl_set_id": ["e637fb20-6a17-4522-810a-990bf1409732"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (64850-840-01)", "package_ndc": "64850-840-01", "marketing_start_date": "20051026"}], "brand_name": "Dantrolene Sodium", "product_id": "64850-840_e3fc6ec6-cdde-456a-81bd-8ebd07065afc", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "64850-840", "generic_name": "dantrolene sodium", "labeler_name": "Elite Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dantrolene Sodium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "25 mg/1"}], "application_number": "ANDA076686", "marketing_category": "ANDA", "marketing_start_date": "20051026", "listing_expiration_date": "20261231"}