Package 51655-594-52

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 51655-594-52
Digits Only 5165559452
Product NDC 51655-594
Product ID 51655-594_494f01b2-8512-f5a5-e063-6294a90ab408
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-594-52)

Marketing

Marketing Status
Marketed Since 2021-02-03
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": "494f01b2-8512-f5a5-e063-6294a90ab408", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["db0e9c21-dc25-629a-e053-2a95a90a5ac3"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-594-52)", "package_ndc": "51655-594-52", "marketing_start_date": "20210203"}], "brand_name": "Pravastatin Sodium", "product_id": "51655-594_494f01b2-8512-f5a5-e063-6294a90ab408", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "51655-594", "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": "ANDA077987", "marketing_category": "ANDA", "marketing_start_date": "20210203", "listing_expiration_date": "20271231"}