valsartan

Generic: valsartan

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler ascend laboratories, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valsartan 160 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-417
Product ID 67877-417_b24a6cf6-a1b4-4d30-8a87-ec5ad793de42
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205536
Listing Expiration 2026-12-31
Marketing Start 2019-03-14

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 67877417
Hyphenated Format 67877-417

Supplemental Identifiers

RxCUI
349199 349200 349201 349483
UPC
0367877418902
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 ANDA205536 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 160 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (67877-417-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (67877-417-10)
  • 90 TABLET, FILM COATED in 1 BOTTLE (67877-417-90)
source: ndc

Packages (3)

67877-417-05 500 TABLET, FILM COATED in 1 BOTTLE (67877-417-05) 67877-417-10 1000 TABLET, FILM COATED in 1 BOTTLE (67877-417-10) 67877-417-90 90 TABLET, FILM COATED in 1 BOTTLE (67877-417-90)

Ingredients (1)

valsartan (160 mg/1)

Linked Drug Pages (1)

Valsartan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b24a6cf6-a1b4-4d30-8a87-ec5ad793de42", "openfda": {"nui": ["N0000000070", "N0000175561"], "upc": ["0367877418902"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349200", "349201", "349483"], "spl_set_id": ["7b4ecaf9-e84c-4660-9cd1-65a238efd8a8"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-417-05)", "package_ndc": "67877-417-05", "marketing_start_date": "20190314"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (67877-417-10)", "package_ndc": "67877-417-10", "marketing_start_date": "20190314"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (67877-417-90)", "package_ndc": "67877-417-90", "marketing_start_date": "20190314"}], "brand_name": "Valsartan", "product_id": "67877-417_b24a6cf6-a1b4-4d30-8a87-ec5ad793de42", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "67877-417", "generic_name": "Valsartan", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "160 mg/1"}], "application_number": "ANDA205536", "marketing_category": "ANDA", "marketing_start_date": "20190314", "listing_expiration_date": "20261231"}