ambrisentan
Generic: ambrisentan
Labeler: zydus pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
ambrisentan
Generic Name
ambrisentan
Labeler
zydus pharmaceuticals usa inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
ambrisentan 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70710-1180
Product ID
70710-1180_4ad0e26d-a3b2-47d1-89a0-6e7e0697d5e4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210058
Listing Expiration
2026-12-31
Marketing Start
2019-04-12
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707101180
Hyphenated Format
70710-1180
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ambrisentan (source: ndc)
Generic Name
ambrisentan (source: ndc)
Application Number
ANDA210058 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET, FILM COATED in 1 BOTTLE (70710-1180-1)
- 30 TABLET, FILM COATED in 1 BOTTLE (70710-1180-3)
- 1 BLISTER PACK in 1 CARTON (70710-1180-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK
- 3 BLISTER PACK in 1 CARTON (70710-1180-8) / 10 TABLET, FILM COATED in 1 BLISTER PACK
- 90 TABLET, FILM COATED in 1 BOTTLE (70710-1180-9)
Packages (5)
70710-1180-1
100 TABLET, FILM COATED in 1 BOTTLE (70710-1180-1)
70710-1180-3
30 TABLET, FILM COATED in 1 BOTTLE (70710-1180-3)
70710-1180-7
1 BLISTER PACK in 1 CARTON (70710-1180-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70710-1180-8
3 BLISTER PACK in 1 CARTON (70710-1180-8) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70710-1180-9
90 TABLET, FILM COATED in 1 BOTTLE (70710-1180-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ad0e26d-a3b2-47d1-89a0-6e7e0697d5e4", "openfda": {"nui": ["N0000175581", "N0000175364"], "unii": ["HW6NV07QEC"], "rxcui": ["722116", "722122"], "spl_set_id": ["37af3191-0ed3-4783-8747-065f1462f2d2"], "pharm_class_epc": ["Endothelin Receptor Antagonist [EPC]"], "pharm_class_moa": ["Endothelin Receptor Antagonists [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1180-1)", "package_ndc": "70710-1180-1", "marketing_start_date": "20190412"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70710-1180-3)", "package_ndc": "70710-1180-3", "marketing_start_date": "20190412"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (70710-1180-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70710-1180-7", "marketing_start_date": "20190412"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70710-1180-8) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70710-1180-8", "marketing_start_date": "20190412"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70710-1180-9)", "package_ndc": "70710-1180-9", "marketing_start_date": "20190412"}], "brand_name": "Ambrisentan", "product_id": "70710-1180_4ad0e26d-a3b2-47d1-89a0-6e7e0697d5e4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Endothelin Receptor Antagonist [EPC]", "Endothelin Receptor Antagonists [MoA]"], "product_ndc": "70710-1180", "generic_name": "Ambrisentan", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ambrisentan", "active_ingredients": [{"name": "AMBRISENTAN", "strength": "10 mg/1"}], "application_number": "ANDA210058", "marketing_category": "ANDA", "marketing_start_date": "20190412", "listing_expiration_date": "20261231"}