sacubitril and valsartan

Generic: sacubitril and valsartan

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sacubitril and valsartan
Generic Name sacubitril and valsartan
Labeler macleods pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sacubitril 97 mg/1, valsartan 103 mg/1

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-572
Product ID 33342-572_103c39e2-f3c8-40fc-a57e-3af018fb4af4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213728
Listing Expiration 2026-12-31
Marketing Start 2024-10-16

Pharmacologic Class

Established (EPC)
angiotensin 2 receptor blocker [epc]
Mechanism of Action
angiotensin 2 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 33342572
Hyphenated Format 33342-572

Supplemental Identifiers

RxCUI
1656340 1656349 1656354
UPC
0333342570574 0333342570093 0333342571571 0333342571090 0333342572097
UNII
80M03YXJ7I 17ERJ0MKGI
NUI
N0000000070 N0000175561

Packaging Origin

Original Packager
true

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 ANDA213728 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 97 mg/1
  • 103 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (33342-572-09)
  • 180 TABLET in 1 BOTTLE (33342-572-57)
source: ndc

Packages (2)

Ingredients (2)

sacubitril (97 mg/1) valsartan (103 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "103c39e2-f3c8-40fc-a57e-3af018fb4af4", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0333342570574", "0333342570093", "0333342571571", "0333342571090", "0333342572097"], "unii": ["80M03YXJ7I", "17ERJ0MKGI"], "rxcui": ["1656340", "1656349", "1656354"], "spl_set_id": ["103c39e2-f3c8-40fc-a57e-3af018fb4af4"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (33342-572-09)", "package_ndc": "33342-572-09", "marketing_start_date": "20241016"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (33342-572-57)", "package_ndc": "33342-572-57", "marketing_start_date": "20241016"}], "brand_name": "Sacubitril and Valsartan", "product_id": "33342-572_103c39e2-f3c8-40fc-a57e-3af018fb4af4", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Neprilysin Inhibitor [EPC]", "Neprilysin Inhibitors [MoA]"], "product_ndc": "33342-572", "generic_name": "Sacubitril and Valsartan", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sacubitril and Valsartan", "active_ingredients": [{"name": "SACUBITRIL", "strength": "97 mg/1"}, {"name": "VALSARTAN", "strength": "103 mg/1"}], "application_number": "ANDA213728", "marketing_category": "ANDA", "marketing_start_date": "20241016", "listing_expiration_date": "20261231"}