Package 51655-708-52

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 51655-708-52
Digits Only 5165570852
Product NDC 51655-708
Product ID 51655-708_4951021b-e7bd-d11f-e063-6294a90aa15f
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-708-52)

Marketing

Marketing Status
Marketed Since 2021-05-21
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (1)

PRAVASTATIN SODIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4951021b-e7bd-d11f-e063-6294a90aa15f", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["db5b8821-dca8-9322-e053-2a95a90abdc3"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-708-52)", "package_ndc": "51655-708-52", "marketing_start_date": "20210521"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "51655-708_4951021b-e7bd-d11f-e063-6294a90aa15f", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "51655-708", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20210521", "listing_expiration_date": "20271231"}