Package 62135-848-90

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 62135-848-90
Digits Only 6213584890
Product NDC 62135-848
Description

90 TABLET, FILM COATED in 1 BOTTLE (62135-848-90)

Marketing

Marketing Status
Marketed Since 2024-09-26
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 (62135-848-90)", "package_ndc": "62135-848-90", "marketing_start_date": "20240926"}], "brand_name": "Pravastatin Sodium", "product_id": "62135-848_2cf16f1b-c67f-455e-e063-6394a90adc0a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "62135-848", "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": "20 mg/1"}], "application_number": "ANDA077917", "marketing_category": "ANDA", "marketing_start_date": "20240926", "listing_expiration_date": "20261231"}