Package 62135-850-90
Brand: pravastatin sodium
Generic: pravastatin sodiumPackage Facts
Identity
Package NDC
62135-850-90
Digits Only
6213585090
Product NDC
62135-850
Description
90 TABLET, FILM COATED in 1 BOTTLE (62135-850-90)
Marketing
Marketing Status
Brand
pravastatin sodium
Generic
pravastatin sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cf16f1b-c67f-455e-e063-6394a90adc0a", "openfda": {"upc": ["0362135850906", "0362135848903", "0362135847906", "0362135849900"], "unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475", "904481"], "spl_set_id": ["f87016fb-4c01-4279-8cf7-59819971ca15"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-850-90)", "package_ndc": "62135-850-90", "marketing_start_date": "20240926"}], "brand_name": "Pravastatin Sodium", "product_id": "62135-850_2cf16f1b-c67f-455e-e063-6394a90adc0a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "62135-850", "generic_name": "Pravastatin Sodium", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "80 mg/1"}], "application_number": "ANDA077917", "marketing_category": "ANDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}