dantrolene sodium
Generic: dantrolene sodium
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
dantrolene sodium
Generic Name
dantrolene sodium
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
dantrolene sodium 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-2169
Product ID
63629-2169_0eb42fdc-2b82-4720-a7aa-24dbc4be869c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA017443
Listing Expiration
2026-12-31
Marketing Start
2016-03-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636292169
Hyphenated Format
63629-2169
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
NDA017443 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (63629-2169-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0eb42fdc-2b82-4720-a7aa-24dbc4be869c", "openfda": {"unii": ["287M0347EV"], "rxcui": ["856660"], "spl_set_id": ["db715aef-83ca-4608-befa-8288ab4adeea"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (63629-2169-1)", "package_ndc": "63629-2169-1", "marketing_start_date": "20210311"}], "brand_name": "dantrolene sodium", "product_id": "63629-2169_0eb42fdc-2b82-4720-a7aa-24dbc4be869c", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Striated Muscle Contraction [PE]", "Decreased Striated Muscle Tone [PE]", "Skeletal Muscle Relaxant [EPC]"], "product_ndc": "63629-2169", "generic_name": "dantrolene sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "dantrolene sodium", "active_ingredients": [{"name": "DANTROLENE SODIUM", "strength": "50 mg/1"}], "application_number": "NDA017443", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160328", "listing_expiration_date": "20261231"}