lovastatin

Generic: lovastatin

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

Drug Facts

Product Profile

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

lovastatin 20 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-468
Product ID 68180-468_99f02cd1-62f8-4398-b07f-44b76f7d9889
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 68180468
Hyphenated Format 68180-468

Supplemental Identifiers

RxCUI
197903 197904 197905
UPC
0368180469070 0368180467076 0368180468073
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 ANDA078296 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68180-468-01)
  • 1000 TABLET in 1 BOTTLE (68180-468-03)
  • 5000 TABLET in 1 BOTTLE (68180-468-05)
  • 60 TABLET in 1 BOTTLE (68180-468-07)
source: ndc

Packages (4)

68180-468-01 100 TABLET in 1 BOTTLE (68180-468-01) 68180-468-03 1000 TABLET in 1 BOTTLE (68180-468-03) 68180-468-05 5000 TABLET in 1 BOTTLE (68180-468-05) 68180-468-07 60 TABLET in 1 BOTTLE (68180-468-07)

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": "99f02cd1-62f8-4398-b07f-44b76f7d9889", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0368180469070", "0368180467076", "0368180468073"], "unii": ["9LHU78OQFD"], "rxcui": ["197903", "197904", "197905"], "spl_set_id": ["df7ddf4f-d569-431e-81f1-9129d7043150"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68180-468-01)", "package_ndc": "68180-468-01", "marketing_start_date": "20071101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68180-468-03)", "package_ndc": "68180-468-03", "marketing_start_date": "20071101"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (68180-468-05)", "package_ndc": "68180-468-05", "marketing_start_date": "20071101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68180-468-07)", "package_ndc": "68180-468-07", "marketing_start_date": "20071101"}], "brand_name": "Lovastatin", "product_id": "68180-468_99f02cd1-62f8-4398-b07f-44b76f7d9889", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68180-468", "generic_name": "lovastatin", "labeler_name": "Lupin Pharmaceuticals, Inc.", "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"}