Package 43063-983-30

Brand: lovastatin

Generic: lovastatin
NDC Package

Package Facts

Identity

Package NDC 43063-983-30
Digits Only 4306398330
Product NDC 43063-983
Description

30 TABLET in 1 BOTTLE, PLASTIC (43063-983-30)

Marketing

Marketing Status
Marketed Since 2019-05-07
Brand lovastatin
Generic lovastatin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "303a95e4-2598-7d25-e063-6294a90a5d2a", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0343063983300"], "unii": ["9LHU78OQFD"], "rxcui": ["197904"], "spl_set_id": ["c37206ae-52f1-4192-9ab9-3044247cf58d"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-983-30)", "package_ndc": "43063-983-30", "marketing_start_date": "20190507"}], "brand_name": "Lovastatin", "product_id": "43063-983_303a95e4-2598-7d25-e063-6294a90a5d2a", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "43063-983", "generic_name": "Lovastatin", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "20 mg/1"}], "application_number": "ANDA075991", "marketing_category": "ANDA", "marketing_start_date": "20021125", "listing_expiration_date": "20261231"}