valsartan

Generic: valsartan

Labeler: avkare
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler avkare
Dosage Form TABLET
Routes
ORAL
Active Ingredients

valsartan 80 mg/1

Manufacturer
AvKARE

Identifiers & Regulatory

Product NDC 42291-857
Product ID 42291-857_488420ae-b4b5-d0ab-e063-6394a90a89bf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204011
Listing Expiration 2027-12-31
Marketing Start 2020-06-23

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 42291857
Hyphenated Format 42291-857

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UNII
80M03YXJ7I
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 valsartan (source: ndc)
Generic Name valsartan (source: ndc)
Application Number ANDA204011 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (42291-857-90)
source: ndc

Packages (1)

Ingredients (1)

valsartan (80 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "488420ae-b4b5-d0ab-e063-6394a90a89bf", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["a8c61488-4219-dfcb-e053-2a95a90a98a4"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["AvKARE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (42291-857-90)", "package_ndc": "42291-857-90", "marketing_start_date": "20200623"}], "brand_name": "Valsartan", "product_id": "42291-857_488420ae-b4b5-d0ab-e063-6394a90a89bf", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "42291-857", "generic_name": "Valsartan", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "80 mg/1"}], "application_number": "ANDA204011", "marketing_category": "ANDA", "marketing_start_date": "20200623", "listing_expiration_date": "20271231"}