Package 51655-834-52

Brand: valsartan

Generic: valsartan
NDC Package

Package Facts

Identity

Package NDC 51655-834-52
Digits Only 5165583452
Product NDC 51655-834
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-834-52)

Marketing

Marketing Status
Marketed Since 2023-02-07
Brand valsartan
Generic valsartan
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4973d0ef-5b55-f2fc-e063-6394a90a988e", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349201"], "spl_set_id": ["f756009f-f04f-6518-e053-6294a90a79ed"], "pharm_class_epc": ["Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-834-52)", "package_ndc": "51655-834-52", "marketing_start_date": "20230207"}], "brand_name": "Valsartan", "product_id": "51655-834_4973d0ef-5b55-f2fc-e063-6394a90a988e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "51655-834", "generic_name": "Valsartan", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan", "active_ingredients": [{"name": "VALSARTAN", "strength": "160 mg/1"}], "application_number": "ANDA203311", "marketing_category": "ANDA", "marketing_start_date": "20230207", "listing_expiration_date": "20271231"}