lovastatin

Generic: lovastatin

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lovastatin
Generic Name lovastatin
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lovastatin 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0762
Product ID 50090-0762_78234f1b-b888-4c09-a204-1b18d6af1f0a
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 500900762
Hyphenated Format 50090-0762

Supplemental Identifiers

RxCUI
197904 197905
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
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-0762-0)
  • 90 TABLET in 1 BOTTLE (50090-0762-2)
source: ndc

Packages (2)

50090-0762-0 30 TABLET in 1 BOTTLE (50090-0762-0) 50090-0762-2 90 TABLET in 1 BOTTLE (50090-0762-2)

Ingredients (1)

lovastatin (40 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": "78234f1b-b888-4c09-a204-1b18d6af1f0a", "openfda": {"nui": ["N0000175589", "N0000000121"], "unii": ["9LHU78OQFD"], "rxcui": ["197904", "197905"], "spl_set_id": ["02aae38d-ee9d-4c09-a155-b69f221ed3e9"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-0762-0)", "package_ndc": "50090-0762-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-0762-2)", "package_ndc": "50090-0762-2", "marketing_start_date": "20141128"}], "brand_name": "Lovastatin", "product_id": "50090-0762_78234f1b-b888-4c09-a204-1b18d6af1f0a", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-0762", "generic_name": "lovastatin", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "40 mg/1"}], "application_number": "ANDA078296", "marketing_category": "ANDA", "marketing_start_date": "20071101", "listing_expiration_date": "20261231"}