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United States · US · US:42794-052_f1f20771-a78f-74cf-e053-2995a90a6adf
AMBRISENTAN
Orange BookUNIISPLATC C02KX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSigmapharm Laboratories, LLC
CountryUS (United States)
ATC codeC02KX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11427940520830 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42794-052-08)
- ndc11427940522210 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42794-052-22)
Annotations
UNII (FDA Substance ID)
HW6NV07QEC
AMBRISENTAN
RxCUI 358274
Orange Book
A208354
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "HW6NV07QEC",
"rxcui": "358274",
"inchikey": "OUJTZYPIHDYQMC-LJQANCHMSA-N",
"display_name": "AMBRISENTAN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"32549c43-f8ff-422c-b42d-ca0877e661cf": {
"match": "brand_token",
"title": "AMBRISENTAN TABLET, FILM COATED [ACTAVIS PHARMA, INC.]",
"spl_version": "19",
"published_date": "2026-04-09"
}
},
"productid": "42794-052_f1f20771-a78f-74cf-e053-2995a90a6adf",
"productndc": "42794-052",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "208354",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "Apr 10, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "002",
"approval_date": "Apr 10, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "AMBRISENTAN",
"proprietary_name": "AMBRISENTAN",
"active_ingred_unit": "mg/1",
"application_number": "ANDA208354",
"marketing_category": "ANDA",
"nonproprietary_name": "AMBRISENTAN",
"start_marketing_date": "20190410",
"active_numerator_strength": "10"
}Related drugs
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