NDC 63629-1019

Lovastatin

Lovastatin

Lovastatin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Lovastatin.

Product ID63629-1019_c18af9e7-b364-4f53-bd54-13b15797c7b5
NDC63629-1019
Product TypeHuman Prescription Drug
Proprietary NameLovastatin
Generic NameLovastatin
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2002-11-25
Marketing CategoryANDA / ANDA
Application NumberANDA075991
Labeler NameBryant Ranch Prepack
Substance NameLOVASTATIN
Active Ingredient Strength20 mg/1
Pharm ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 63629-1019-0

1000 TABLET in 1 BOTTLE (63629-1019-0)
Marketing Start Date2019-05-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-1019-0 [63629101900]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075991
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-14
Inactivation Date2020-01-31

NDC 63629-1019-2 [63629101902]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075991
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-14
Inactivation Date2020-01-31

NDC 63629-1019-6 [63629101906]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075991
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-14
Inactivation Date2020-01-31

NDC 63629-1019-1 [63629101901]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075991
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-14
Inactivation Date2020-01-31

NDC 63629-1019-3 [63629101903]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075991
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-14
Inactivation Date2020-01-31

NDC 63629-1019-8 [63629101908]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075991
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-14
Inactivation Date2020-01-31

NDC 63629-1019-5 [63629101905]

Lovastatin TABLET
Marketing CategoryANDA
Application NumberANDA075991
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-14
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
LOVASTATIN20 mg/1

OpenFDA Data

SPL SET ID:c871a6a7-67a4-4ac1-b102-3f1604625c7d
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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