Package 70518-0876-0

Brand: pravastatin sodium

Generic: pravastatin sodium
NDC Package

Package Facts

Identity

Package NDC 70518-0876-0
Digits Only 7051808760
Product NDC 70518-0876
Product ID 70518-0876_4846c3d5-f1fe-20dc-e063-6394a90a2a3d
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-0876-0)

Marketing

Marketing Status
Marketed Since 2017-11-29
Brand pravastatin sodium
Generic pravastatin sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4846c3d5-f1fe-20dc-e063-6394a90a2a3d", "openfda": {"unii": ["3M8608UQ61"], "rxcui": ["904475"], "spl_set_id": ["5ecd9fd1-7662-412d-99c5-13c77188748c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-0876-0)", "package_ndc": "70518-0876-0", "marketing_start_date": "20171129"}], "brand_name": "PRAVASTATIN SODIUM", "product_id": "70518-0876_4846c3d5-f1fe-20dc-e063-6394a90a2a3d", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-0876", "generic_name": "PRAVASTATIN SODIUM", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAVASTATIN SODIUM", "active_ingredients": [{"name": "PRAVASTATIN SODIUM", "strength": "40 mg/1"}], "application_number": "ANDA076341", "marketing_category": "ANDA", "marketing_start_date": "20171129", "listing_expiration_date": "20271231"}