lovastatin

Generic: lovastatin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lovastatin
Generic Name lovastatin
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lovastatin 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-993
Product ID 71205-993_e637904d-8af6-47fe-b10e-db813d5531bc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075991
Listing Expiration 2026-12-31
Marketing Start 2002-11-25

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 71205993
Hyphenated Format 71205-993

Supplemental Identifiers

RxCUI
197903 197904 197905
UPC
0371205992309 0371205993306 0371205994303
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 ANDA075991 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71205-993-00)
  • 1000 TABLET in 1 BOTTLE (71205-993-11)
  • 30 TABLET in 1 BOTTLE (71205-993-30)
  • 500 TABLET in 1 BOTTLE (71205-993-55)
  • 60 TABLET in 1 BOTTLE (71205-993-60)
  • 90 TABLET in 1 BOTTLE (71205-993-90)
source: ndc

Packages (6)

71205-993-00 100 TABLET in 1 BOTTLE (71205-993-00) 71205-993-11 1000 TABLET in 1 BOTTLE (71205-993-11) 71205-993-30 30 TABLET in 1 BOTTLE (71205-993-30) 71205-993-55 500 TABLET in 1 BOTTLE (71205-993-55) 71205-993-60 60 TABLET in 1 BOTTLE (71205-993-60) 71205-993-90 90 TABLET in 1 BOTTLE (71205-993-90)

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": "e637904d-8af6-47fe-b10e-db813d5531bc", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0371205992309", "0371205993306", "0371205994303"], "unii": ["9LHU78OQFD"], "rxcui": ["197903", "197904", "197905"], "spl_set_id": ["25efd38a-1495-4824-9137-a3429bc471bd"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71205-993-00)", "package_ndc": "71205-993-00", "marketing_start_date": "20200401"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71205-993-11)", "package_ndc": "71205-993-11", "marketing_start_date": "20200401"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-993-30)", "package_ndc": "71205-993-30", "marketing_start_date": "20200401"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71205-993-55)", "package_ndc": "71205-993-55", "marketing_start_date": "20200401"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-993-60)", "package_ndc": "71205-993-60", "marketing_start_date": "20200401"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-993-90)", "package_ndc": "71205-993-90", "marketing_start_date": "20200401"}], "brand_name": "Lovastatin", "product_id": "71205-993_e637904d-8af6-47fe-b10e-db813d5531bc", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71205-993", "generic_name": "Lovastatin", "labeler_name": "Proficient Rx LP", "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"}