NDC 53489-608

lovastatin

Lovastatin

lovastatin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Mutual Pharmaceutical Company, Inc.. The primary component is Lovastatin.

Product ID53489-608_36f83432-6257-4cda-9902-510ec4b0975c
NDC53489-608
Product TypeHuman Prescription Drug
Proprietary Namelovastatin
Generic NameLovastatin
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2006-04-14
Marketing CategoryANDA / ANDA
Application NumberANDA077520
Labeler NameMutual Pharmaceutical Company, Inc.
Substance NameLOVASTATIN
Active Ingredient Strength20 mg/1
Pharm ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 53489-608-07

30 TABLET in 1 BOTTLE, PLASTIC (53489-608-07)
Marketing Start Date2006-04-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53489-608-03 [53489060803]

lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA077520
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-14
Inactivation Date2019-11-27

NDC 53489-608-10 [53489060810]

lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA077520
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-14
Inactivation Date2019-11-27

NDC 53489-608-07 [53489060807]

lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA077520
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-14
Inactivation Date2019-11-27

NDC 53489-608-05 [53489060805]

lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA077520
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-14
Inactivation Date2019-11-27

NDC 53489-608-06 [53489060806]

lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA077520
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-14
Inactivation Date2019-11-27

NDC 53489-608-01 [53489060801]

lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA077520
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-04-14
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
LOVASTATIN20 mg/1

OpenFDA Data

SPL SET ID:caf7c3af-8256-4557-af40-e8143e9af9f1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197904
  • 197905
  • 197903

    • Pharmacological Class

    • HMG-CoA Reductase Inhibitor [EPC]
    • Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

    NDC Crossover Matching brand name "lovastatin" or generic name "Lovastatin"

    NDCBrand NameGeneric Name
    0093-0576LovastatinLovastatin
    0093-0926LovastatinLovastatin
    0093-0928LovastatinLovastatin
    0185-0070LovastatinLovastatin
    0185-0072LovastatinLovastatin
    0185-0074LovastatinLovastatin
    0440-6694LovastatinLovastatin
    0615-5589LovastatinLovastatin
    0615-6551LovastatinLovastatin
    0615-6590LovastatinLovastatin
    0615-7674LovastatinLovastatin
    0615-7679LovastatinLovastatin
    0615-7685LovastatinLovastatin
    0615-7690LovastatinLovastatin
    0615-8151Lovastatinlovastatin
    0615-8152Lovastatinlovastatin
    10544-235LovastatinLovastatin
    10544-241LovastatinLovastatin
    10544-242LovastatinLovastatin
    10544-246LovastatinLovastatin
    21695-534LovastatinLovastatin
    21695-535LovastatinLovastatin
    21695-536LovastatinLovastatin
    33261-547LovastatinLovastatin
    33261-548LovastatinLovastatin
    33261-549LovastatinLovastatin
    35356-885LovastatinLovastatin
    42254-025LovastatinLovastatin
    42254-028LovastatinLovastatin
    42254-106LovastatinLovastatin
    68001-224LovastatinLovastatin
    68001-315LovastatinLovastatin
    68001-316LovastatinLovastatin
    68001-214LovastatinLovastatin
    68001-314LovastatinLovastatin
    68071-3108LovastatinLovastatin
    68071-1973LovastatinLovastatin
    68071-3127LovastatinLovastatin
    68071-3261LovastatinLovastatin
    68071-3397LovastatinLovastatin
    68071-4271LovastatinLovastatin
    68084-559LovastatinLovastatin
    68180-468LovastatinLovastatin
    68180-467LovastatinLovastatin
    68180-469LovastatinLovastatin
    68645-576LovastatinLovastatin
    68645-566LovastatinLovastatin
    68788-2634LovastatinLovastatin
    68645-567LovastatinLovastatin
    68788-0926LovastatinLovastatin
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