valsartan
Generic: valsartan
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
valsartan
Generic Name
valsartan
Labeler
american health packaging
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
valsartan 80 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-623
Product ID
60687-623_23562661-facc-865c-e063-6394a90af4c0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205536
Listing Expiration
2026-12-31
Marketing Start
2021-06-29
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687623
Hyphenated Format
60687-623
Supplemental Identifiers
RxCUI
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
valsartan (source: ndc)
Generic Name
valsartan (source: ndc)
Application Number
ANDA205536 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-623-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-623-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "23562661-facc-865c-e063-6394a90af4c0", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349199", "349201", "349483"], "spl_set_id": ["7ea2fdf1-4fda-47a7-8110-62fb6468c989"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-623-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-623-11)", "package_ndc": "60687-623-01", "marketing_start_date": "20210629"}], "brand_name": "Valsartan", "product_id": "60687-623_23562661-facc-865c-e063-6394a90af4c0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "60687-623", "generic_name": "Valsartan", "labeler_name": "American Health Packaging", "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": "20210629", "listing_expiration_date": "20261231"}