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United States · US · US:50268-217_32f9f951-bf56-47f2-e063-6394a90a9c6d
Dantrolene Sodium
Orange BookUNIISPLATC M03CA01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAvPAK
CountryUS (United States)
ATC codeM03CA01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11502682171550 BLISTER PACK in 1 BOX (50268-217-15) / 1 CAPSULE in 1 BLISTER PACK (50268-217-11)
Annotations
UNII (FDA Substance ID)
287M0347EV
DANTROLENE SODIUM
RxCUI 3106
Orange Book
A076856
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "287M0347EV",
"rxcui": "3106",
"inchikey": "LTWQNYPDAUSXBC-CDJGKPBYSA-L",
"display_name": "DANTROLENE SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c3c45b27-f786-456e-95d6-2e38ef36190a": {
"match": "brand_token",
"title": "DANTROLENE SODIUM CAPSULE [AMNEAL PHARMACEUTICALS OF NEW YORK LLC]",
"spl_version": "15",
"published_date": "2026-04-30"
}
},
"productid": "50268-217_32f9f951-bf56-47f2-e063-6394a90a9c6d",
"productndc": "50268-217",
"dosage_form": "CAPSULE",
"orange_book": {
"appl_no": "076856",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "25MG",
"product_no": "001",
"approval_date": "Mar 1, 2005"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "50MG",
"product_no": "002",
"approval_date": "Mar 1, 2005"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "100MG",
"product_no": "003",
"approval_date": "Mar 1, 2005"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DANTROLENE SODIUM",
"proprietary_name": "Dantrolene Sodium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA076856",
"marketing_category": "ANDA",
"nonproprietary_name": "Dantrolene Sodium",
"start_marketing_date": "20210309",
"active_numerator_strength": "25"
}Related drugs
Other records sharing ATC code M03CA01.
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