Package 82009-014-10

Brand: simvastatin

Generic: simvastatin
NDC Package

Package Facts

Identity

Package NDC 82009-014-10
Digits Only 8200901410
Product NDC 82009-014
Product ID 82009-014_1de47781-9000-0fc1-e063-6294a90a8139
Description

1000 TABLET, FILM COATED in 1 BOTTLE (82009-014-10)

Marketing

Marketing Status
Marketed Since 2022-05-26
Brand simvastatin
Generic simvastatin
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": "1de47781-9000-0fc1-e063-6294a90a8139", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0382009015101", "0382009013107", "0382009014104", "0382009012100"], "unii": ["AGG2FN16EV"], "rxcui": ["198211", "200345", "312961", "312962", "314231"], "spl_set_id": ["2b4255a7-f9f5-4235-8dbb-b0f03acbd624"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (82009-014-10)", "package_ndc": "82009-014-10", "marketing_start_date": "20220526"}], "brand_name": "Simvastatin", "product_id": "82009-014_1de47781-9000-0fc1-e063-6294a90a8139", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "82009-014", "generic_name": "Simvastatin", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Simvastatin", "active_ingredients": [{"name": "SIMVASTATIN", "strength": "20 mg/1"}], "application_number": "ANDA200895", "marketing_category": "ANDA", "marketing_start_date": "20220526", "listing_expiration_date": "20261231"}