sacubitril and valsartan
Generic: sacubitril and valsartan
Labeler: avkareDrug Facts
Product Profile
Brand Name
sacubitril and valsartan
Generic Name
sacubitril and valsartan
Labeler
avkare
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
sacubitril 49 mg/1, valsartan 51 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
73190-006
Product ID
73190-006_4c260039-9848-e878-e063-6294a90a3dcb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213748
Listing Expiration
2027-12-31
Marketing Start
2025-01-21
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73190006
Hyphenated Format
73190-006
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA213748 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 49 mg/1
- 51 mg/1
Packaging
- 1000 TABLET, FILM COATED in 1 BOTTLE (73190-006-10)
- 180 TABLET, FILM COATED in 1 BOTTLE (73190-006-18)
- 60 TABLET, FILM COATED in 1 BOTTLE (73190-006-60)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c260039-9848-e878-e063-6294a90a3dcb", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0373190002186", "0373190001189", "0373190002605", "0373190003602", "0373190001608", "0373190003183"], "unii": ["80M03YXJ7I", "17ERJ0MKGI"], "rxcui": ["1656340", "1656349", "1656354"], "spl_set_id": ["2c39c326-34a2-b7f4-e063-6294a90a6732"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (73190-006-10)", "package_ndc": "73190-006-10", "marketing_start_date": "20260225"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (73190-006-18)", "package_ndc": "73190-006-18", "marketing_start_date": "20250121"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (73190-006-60)", "package_ndc": "73190-006-60", "marketing_start_date": "20250121"}], "brand_name": "Sacubitril and Valsartan", "product_id": "73190-006_4c260039-9848-e878-e063-6294a90a3dcb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Neprilysin Inhibitor [EPC]", "Neprilysin Inhibitors [MoA]"], "product_ndc": "73190-006", "generic_name": "Sacubitril and Valsartan", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sacubitril and Valsartan", "active_ingredients": [{"name": "SACUBITRIL", "strength": "49 mg/1"}, {"name": "VALSARTAN", "strength": "51 mg/1"}], "application_number": "ANDA213748", "marketing_category": "ANDA", "marketing_start_date": "20250121", "listing_expiration_date": "20271231"}