Package 50268-665-15

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 50268-665-15
Digits Only 5026866515
Product NDC 50268-665
Description

50 BLISTER PACK in 1 BOX (50268-665-15) / 1 TABLET in 1 BLISTER PACK (50268-665-11)

Marketing

Marketing Status
Marketed Since 2021-02-01
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": "47fb4c90-456b-508c-e063-6394a90a5da5", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904458", "904467", "904475", "904481"], "spl_set_id": ["ba4ac602-46fa-8386-e053-2995a90a9764"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-665-15)  / 1 TABLET in 1 BLISTER PACK (50268-665-11)", "package_ndc": "50268-665-15", "marketing_start_date": "20210201"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "50268-665_47fb4c90-456b-508c-e063-6394a90a5da5", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50268-665", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20210201", "listing_expiration_date": "20271231"}