valsartan

Generic: valsartan

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name valsartan
Generic Name valsartan
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

valsartan 80 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-550
Product ID 72189-550_170427e5-c74d-c7fc-e063-6294a90a6860
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205536
Listing Expiration 2026-12-31
Marketing Start 2024-04-26

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 72189550
Hyphenated Format 72189-550

Supplemental Identifiers

RxCUI
349199
UNII
80M03YXJ7I
NUI
N0000000070 N0000175561

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
  • 80 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-550-30)
source: ndc

Packages (1)

72189-550-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-550-30)

Ingredients (1)

valsartan (80 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": "170427e5-c74d-c7fc-e063-6294a90a6860", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349199"], "spl_set_id": ["170427e5-c74c-c7fc-e063-6294a90a6860"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-550-30)", "package_ndc": "72189-550-30", "marketing_start_date": "20240426"}], "brand_name": "Valsartan", "product_id": "72189-550_170427e5-c74d-c7fc-e063-6294a90a6860", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-550", "generic_name": "Valsartan", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "80 mg/1"}], "application_number": "ANDA205536", "marketing_category": "ANDA", "marketing_start_date": "20240426", "listing_expiration_date": "20261231"}