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 71205-440
Product ID 71205-440_027bd594-6a0a-4e6d-bd3c-4f33fdb4166a
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 71205440
Hyphenated Format 71205-440

Supplemental Identifiers

RxCUI
197904
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 ANDA075551 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-440-30)
  • 60 TABLET in 1 BOTTLE (71205-440-60)
  • 90 TABLET in 1 BOTTLE (71205-440-90)
source: ndc

Packages (3)

71205-440-30 30 TABLET in 1 BOTTLE (71205-440-30) 71205-440-60 60 TABLET in 1 BOTTLE (71205-440-60) 71205-440-90 90 TABLET in 1 BOTTLE (71205-440-90)

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": "027bd594-6a0a-4e6d-bd3c-4f33fdb4166a", "openfda": {"nui": ["N0000175589", "N0000000121"], "unii": ["9LHU78OQFD"], "rxcui": ["197904"], "spl_set_id": ["027bd594-6a0a-4e6d-bd3c-4f33fdb4166a"], "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": "30 TABLET in 1 BOTTLE (71205-440-30)", "package_ndc": "71205-440-30", "marketing_start_date": "20200401"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-440-60)", "package_ndc": "71205-440-60", "marketing_start_date": "20200401"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-440-90)", "package_ndc": "71205-440-90", "marketing_start_date": "20200401"}], "brand_name": "Lovastatin", "product_id": "71205-440_027bd594-6a0a-4e6d-bd3c-4f33fdb4166a", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71205-440", "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": "ANDA075551", "marketing_category": "ANDA", "marketing_start_date": "20011217", "listing_expiration_date": "20261231"}