lovastatin

Generic: lovastatin

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lovastatin
Generic Name lovastatin
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lovastatin 10 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-0926
Product ID 0093-0926_caf8172a-311b-447a-8c8b-e9d70c23c8e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075551
Listing Expiration 2026-12-31
Marketing Start 2001-12-17

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 00930926
Hyphenated Format 0093-0926

Supplemental Identifiers

RxCUI
197903 197904 197905
UNII
9LHU78OQFD
NUI
N0000175589 N0000000121

Packaging Origin

Original Packager
true

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 ANDA075551 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (0093-0926-06)
  • 1000 TABLET in 1 BOTTLE (0093-0926-10)
source: ndc

Packages (2)

0093-0926-06 60 TABLET in 1 BOTTLE (0093-0926-06) 0093-0926-10 1000 TABLET in 1 BOTTLE (0093-0926-10)

Ingredients (1)

lovastatin (10 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": "caf8172a-311b-447a-8c8b-e9d70c23c8e8", "openfda": {"nui": ["N0000175589", "N0000000121"], "unii": ["9LHU78OQFD"], "rxcui": ["197903", "197904", "197905"], "spl_set_id": ["0e15feec-d27e-4861-8152-c5a8b8ccacd4"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (0093-0926-06)", "package_ndc": "0093-0926-06", "marketing_start_date": "20011217"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0093-0926-10)", "package_ndc": "0093-0926-10", "marketing_start_date": "20011217"}], "brand_name": "Lovastatin", "product_id": "0093-0926_caf8172a-311b-447a-8c8b-e9d70c23c8e8", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "0093-0926", "generic_name": "Lovastatin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lovastatin", "active_ingredients": [{"name": "LOVASTATIN", "strength": "10 mg/1"}], "application_number": "ANDA075551", "marketing_category": "ANDA", "marketing_start_date": "20011217", "listing_expiration_date": "20261231"}