dantrolene sodium
Generic: dantrolene sodium
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
dantrolene sodium
Generic Name
dantrolene sodium
Labeler
american health packaging
Dosage Form
CAPSULE
Routes
Active Ingredients
dantrolene sodium 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68084-300
Product ID
68084-300_259da864-9b15-9e66-e063-6294a90a9b4b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076856
Listing Expiration
2026-12-31
Marketing Start
2008-09-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68084300
Hyphenated Format
68084-300
Supplemental Identifiers
RxCUI
UNII
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
ANDA076856 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-300-21) / 1 CAPSULE in 1 BLISTER PACK (68084-300-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "259da864-9b15-9e66-e063-6294a90a9b4b", "openfda": {"unii": ["287M0347EV"], "rxcui": ["856656"], "spl_set_id": ["5162f162-8454-4c07-9670-682df7c30b0f"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-300-21) / 1 CAPSULE in 1 BLISTER PACK (68084-300-11)", "package_ndc": "68084-300-21", "marketing_start_date": "20080929"}], "brand_name": "Dantrolene Sodium", "product_id": "68084-300_259da864-9b15-9e66-e063-6294a90a9b4b", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "68084-300", "generic_name": "Dantrolene Sodium", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dantrolene Sodium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "25 mg/1"}], "application_number": "ANDA076856", "marketing_category": "ANDA", "marketing_start_date": "20080929", "listing_expiration_date": "20261231"}