Package 51655-244-52

Brand: valsartan

Generic: valsartan
NDC Package

Package Facts

Identity

Package NDC 51655-244-52
Digits Only 5165524452
Product NDC 51655-244
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-244-52)

Marketing

Marketing Status
Marketed Since 2022-10-27
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": "48e6b6eb-c158-aeec-e063-6294a90abae3", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349201"], "spl_set_id": ["f2b77f2f-333e-f3e3-e053-2a95a90a1fa7"], "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 (51655-244-52)", "package_ndc": "51655-244-52", "marketing_start_date": "20221027"}], "brand_name": "Valsartan", "product_id": "51655-244_48e6b6eb-c158-aeec-e063-6294a90abae3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "51655-244", "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": "ANDA090866", "marketing_category": "ANDA", "marketing_start_date": "20221027", "listing_expiration_date": "20271231"}