NDC 68788-9182

Lovastatin

Lovastatin

Lovastatin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Preferred Pharmaceuticals, Inc. The primary component is Lovastatin.

Product ID68788-9182_10732fde-1cf5-4001-8c92-e7df59db22fa
NDC68788-9182
Product TypeHuman Prescription Drug
Proprietary NameLovastatin
Generic NameLovastatin
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2005-10-27
Marketing CategoryANDA / ANDA
Application NumberANDA075828
Labeler NamePreferred Pharmaceuticals, Inc
Substance NameLOVASTATIN
Active Ingredient Strength40 mg/1
Pharm ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 68788-9182-9

90 TABLET in 1 BOTTLE, DISPENSING (68788-9182-9)
Marketing Start Date2011-10-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-9182-6 [68788918206]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075828
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-10-05
Inactivation Date2020-01-31

NDC 68788-9182-3 [68788918203]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075828
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-10-05
Inactivation Date2020-01-31

NDC 68788-9182-1 [68788918201]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075828
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-10-05
Inactivation Date2020-01-31

NDC 68788-9182-9 [68788918209]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075828
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-10-05
Inactivation Date2020-01-31

NDC 68788-9182-8 [68788918208]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075828
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-10-27
Marketing End Date2013-03-18

Drug Details

Active Ingredients

IngredientStrength
LOVASTATIN40 mg/1

OpenFDA Data

SPL SET ID:b1f9a948-f807-4256-b221-e431167f9d54
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197905
  • 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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