Package 51655-456-52

Brand: valsartan

Generic: valsartan
NDC Package

Package Facts

Identity

Package NDC 51655-456-52
Digits Only 5165545652
Product NDC 51655-456
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-456-52)

Marketing

Marketing Status
Marketed Since 2020-10-23
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": "490ef62b-2445-2161-e063-6294a90a748d", "openfda": {"nui": ["N0000000070", "N0000175561"], "unii": ["80M03YXJ7I"], "rxcui": ["349201"], "spl_set_id": ["f305e9d7-341a-45f6-e053-2a95a90a2d69"], "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 (51655-456-52)", "package_ndc": "51655-456-52", "marketing_start_date": "20201023"}], "brand_name": "Valsartan", "product_id": "51655-456_490ef62b-2445-2161-e063-6294a90a748d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "51655-456", "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": "ANDA202696", "marketing_category": "ANDA", "marketing_start_date": "20201023", "listing_expiration_date": "20271231"}