Package 0480-7270-98
Brand: pravastatin sodium
Generic: pravastatin sodiumPackage Facts
Identity
Package NDC
0480-7270-98
Digits Only
0480727098
Product NDC
0480-7270
Description
90 TABLET in 1 BOTTLE (0480-7270-98)
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": "95e8c960-5096-43a9-8807-89cdf404a214", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904481"], "spl_set_id": ["f66cb1c1-5ff1-4b0b-89d0-8ecaee26b0b8"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (0480-7270-10)", "package_ndc": "0480-7270-10", "marketing_start_date": "20230320"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0480-7270-98)", "package_ndc": "0480-7270-98", "marketing_start_date": "20230209"}], "brand_name": "Pravastatin Sodium", "product_id": "0480-7270_95e8c960-5096-43a9-8807-89cdf404a214", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0480-7270", "generic_name": "Pravastatin Sodium", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pravastatin Sodium", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "80 mg/1"}], "application_number": "ANDA077793", "marketing_category": "ANDA", "marketing_start_date": "20230209", "listing_expiration_date": "20261231"}