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United States · US · US:0615-8611_1a937beb-d2a1-4ea1-8e06-e0c87b357168
Ranolazine
Orange BookUNIISPLATC C01EB18
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
CountryUS (United States)
ATC codeC01EB18
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11061586113930 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8611-39)
Annotations
UNII (FDA Substance ID)
A6IEZ5M406
RANOLAZINE
RxCUI 35829
Orange Book
A210188
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "A6IEZ5M406",
"rxcui": "35829",
"inchikey": "XKLMZUWKNUAPSZ-UHFFFAOYSA-N",
"display_name": "RANOLAZINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"d2454377-2abd-4d9f-85f1-12f1adbb10e5": {
"match": "brand_token",
"title": "RANOLAZINE TABLET, FILM COATED, EXTENDED RELEASE [TORRENT PHARMA, INC.]",
"spl_version": "1",
"published_date": "2026-05-12"
}
},
"productid": "0615-8611_1a937beb-d2a1-4ea1-8e06-e0c87b357168",
"productndc": "0615-8611",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "210188",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "500MG",
"product_no": "001",
"approval_date": "Aug 19, 2019"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "1GM",
"product_no": "002",
"approval_date": "Aug 19, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "RANOLAZINE",
"proprietary_name": "Ranolazine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210188",
"marketing_category": "ANDA",
"nonproprietary_name": "Ranolazine",
"start_marketing_date": "20190910",
"active_numerator_strength": "500"
}Related drugs
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