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United States · US · US:69097-387_7921a3aa-6e99-4f28-a5d3-a3047b1ec3cc
Ambrisentan
Orange BookUNIISPLATC C02KX02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCipla USA Inc.
CountryUS (United States)
ATC codeC02KX02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11690973870230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-387-02)
- ndc1169097387191 BLISTER PACK in 1 CARTON (69097-387-19) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
HW6NV07QEC
AMBRISENTAN
RxCUI 358274
Orange Book
A210715
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": "69097-387_7921a3aa-6e99-4f28-a5d3-a3047b1ec3cc",
"productndc": "69097-387",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "210715",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "5MG",
"product_no": "001",
"approval_date": "Apr 26, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "10MG",
"product_no": "002",
"approval_date": "Apr 26, 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": "ANDA210715",
"marketing_category": "ANDA",
"nonproprietary_name": "Ambrisentan",
"start_marketing_date": "20190426",
"active_numerator_strength": "10"
}Related drugs
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