lovastatin

Generic: lovastatin

Labeler: legacy pharmaceutical packaging, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lovastatin
Generic Name lovastatin
Labeler legacy pharmaceutical packaging, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lovastatin 20 mg/1

Manufacturer
Legacy Pharmaceutical Packaging, LLC

Identifiers & Regulatory

Product NDC 68645-566
Product ID 68645-566_3300208d-97e4-6182-e063-6394a90ab2fb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078296
Listing Expiration 2026-12-31
Marketing Start 2007-11-01

Pharmacologic Class

Established (EPC)
hmg-coa reductase inhibitor [epc]
Mechanism of Action
hydroxymethylglutaryl-coa reductase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68645566
Hyphenated Format 68645-566

Supplemental Identifiers

RxCUI
197904 197905
UPC
0368645566900 0368645567907
UNII
9LHU78OQFD
NUI
N0000175589 N0000000121

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lovastatin (source: ndc)
Generic Name lovastatin (source: ndc)
Application Number ANDA078296 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68645-566-90)
source: ndc

Packages (1)

68645-566-90 90 TABLET in 1 BOTTLE (68645-566-90)

Ingredients (1)

lovastatin (20 mg/1)

Linked Drug Pages (1)

Lovastatin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3300208d-97e4-6182-e063-6394a90ab2fb", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0368645566900", "0368645567907"], "unii": ["9LHU78OQFD"], "rxcui": ["197904", "197905"], "spl_set_id": ["a4f02fa1-3281-46fa-bd52-323e2644b6f8"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68645-566-90)", "package_ndc": "68645-566-90", "marketing_start_date": "20071101"}], "brand_name": "Lovastatin", "product_id": "68645-566_3300208d-97e4-6182-e063-6394a90ab2fb", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68645-566", "generic_name": "lovastatin", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "20 mg/1"}], "application_number": "ANDA078296", "marketing_category": "ANDA", "marketing_start_date": "20071101", "listing_expiration_date": "20261231"}