sacubitril and valsartan
Generic: sacubitril and valsartan
Labeler: zydus pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
sacubitril and valsartan
Generic Name
sacubitril and valsartan
Labeler
zydus pharmaceuticals usa inc.
Dosage Form
TABLET
Routes
Active Ingredients
sacubitril 24 mg/1, valsartan 26 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70710-1272
Product ID
70710-1272_581c1ab7-7950-4524-a47a-de378f5ee9ec
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213719
Listing Expiration
2026-12-31
Marketing Start
2025-07-08
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
707101272
Hyphenated Format
70710-1272
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
sacubitril and valsartan (source: ndc)
Generic Name
sacubitril and valsartan (source: ndc)
Application Number
ANDA213719 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 24 mg/1
- 26 mg/1
Packaging
- 10 BLISTER PACK in 1 CARTON (70710-1272-4) / 10 TABLET in 1 BLISTER PACK (70710-1272-2)
- 60 TABLET in 1 BOTTLE (70710-1272-6)
- 180 TABLET in 1 BOTTLE (70710-1272-8)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "581c1ab7-7950-4524-a47a-de378f5ee9ec", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I", "17ERJ0MKGI"], "rxcui": ["1656340", "1656349", "1656354"], "spl_set_id": ["4ed0dbe4-8752-43c5-8c28-17c9638a52d6"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70710-1272-4) / 10 TABLET in 1 BLISTER PACK (70710-1272-2)", "package_ndc": "70710-1272-4", "marketing_start_date": "20250708"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (70710-1272-6)", "package_ndc": "70710-1272-6", "marketing_start_date": "20250708"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (70710-1272-8)", "package_ndc": "70710-1272-8", "marketing_start_date": "20250708"}], "brand_name": "sacubitril and valsartan", "product_id": "70710-1272_581c1ab7-7950-4524-a47a-de378f5ee9ec", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Neprilysin Inhibitor [EPC]", "Neprilysin Inhibitors [MoA]"], "product_ndc": "70710-1272", "generic_name": "sacubitril and valsartan", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sacubitril and valsartan", "active_ingredients": [{"name": "SACUBITRIL", "strength": "24 mg/1"}, {"name": "VALSARTAN", "strength": "26 mg/1"}], "application_number": "ANDA213719", "marketing_category": "ANDA", "marketing_start_date": "20250708", "listing_expiration_date": "20261231"}