NDC 68788-7193

Pravastatin sodium

Pravastatin Sodium

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

Product ID68788-7193_77d581ee-7d09-4408-ab06-336c3a8e482e
NDC68788-7193
Product TypeHuman Prescription Drug
Proprietary NamePravastatin sodium
Generic NamePravastatin Sodium
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-07-18
Marketing CategoryANDA / ANDA
Application NumberANDA076714
Labeler NamePreferred Pharmaceuticals Inc.
Substance NamePRAVASTATIN SODIUM
Active Ingredient Strength80 mg/1
Pharm ClassesHMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 68788-7193-3

30 TABLET in 1 BOTTLE (68788-7193-3)
Marketing Start Date2018-07-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-7193-8 [68788719308]

Pravastatin sodium TABLET
Marketing CategoryANDA
Application NumberANDA076714
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-07-18
Marketing End Date2019-11-12

NDC 68788-7193-2 [68788719302]

Pravastatin sodium TABLET
Marketing CategoryANDA
Application NumberANDA076714
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-07-18
Marketing End Date2019-11-12

NDC 68788-7193-1 [68788719301]

Pravastatin sodium TABLET
Marketing CategoryANDA
Application NumberANDA076714
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-07-18
Marketing End Date2019-11-12

NDC 68788-7193-3 [68788719303]

Pravastatin sodium TABLET
Marketing CategoryANDA
Application NumberANDA076714
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-07-18
Marketing End Date2019-11-12

NDC 68788-7193-6 [68788719306]

Pravastatin sodium TABLET
Marketing CategoryANDA
Application NumberANDA076714
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-07-18
Marketing End Date2019-11-12

NDC 68788-7193-9 [68788719309]

Pravastatin sodium TABLET
Marketing CategoryANDA
Application NumberANDA076714
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-07-18
Marketing End Date2019-11-12

Drug Details

Active Ingredients

IngredientStrength
PRAVASTATIN SODIUM80 mg/1

OpenFDA Data

SPL SET ID:77d581ee-7d09-4408-ab06-336c3a8e482e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 904481
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Pravastatin sodium" or generic name "Pravastatin Sodium"

    NDCBrand NameGeneric Name
    0093-0771Pravastatin SodiumPravastatin Sodium
    0093-7201Pravastatin SodiumPravastatin Sodium
    0093-7202Pravastatin SodiumPravastatin Sodium
    0093-7270Pravastatin SodiumPravastatin Sodium
    0615-6556Pravastatin SodiumPravastatin Sodium
    0615-6557Pravastatin SodiumPravastain Sodium
    0615-7740Pravastatin SodiumPravastatin Sodium
    0615-7868PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    0615-7869PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    0615-8029Pravastatin SodiumPravastatin Sodium
    0615-8030Pravastatin SodiumPravastatin Sodium
    68071-2088Pravastatin SodiumPravastatin Sodium
    68071-3247PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68071-3253pravastatin sodiumpravastatin sodium
    68071-1917Pravastatin sodiumPravastatin sodium
    68071-3358PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68071-3361PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68071-2194Pravastatin sodiumPravastatin sodium
    68071-3366PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68071-4039PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68071-4707pravastatin sodiumpravastatin sodium
    68180-488PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68180-487PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68180-486PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68180-485PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68382-071pravastatin sodiumpravastatin sodium
    68382-070pravastatin sodiumpravastatin sodium
    68382-073pravastatin sodiumpravastatin sodium
    68382-072pravastatin sodiumpravastatin sodium
    68462-195Pravastatin SodiumPravastatin Sodium
    68462-198Pravastatin SodiumPravastatin Sodium
    68462-197Pravastatin SodiumPravastatin Sodium
    68462-196Pravastatin SodiumPravastatin Sodium
    68788-7253PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68788-7013PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68788-7193Pravastatin sodiumPravastatin sodium
    68788-7316PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    68788-7413PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    69097-185Pravastatin SodiumPravastatin Sodium
    69097-186Pravastatin SodiumPravastatin Sodium
    69097-183Pravastatin SodiumPravastatin Sodium
    69097-184Pravastatin SodiumPravastatin Sodium
    70518-0304Pravastatin SodiumPravastatin Sodium
    70518-0412PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    70518-0549PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    70518-0707pravastatin sodiumpravastatin sodium
    70518-0423Pravastatin SodiumPravastatin Sodium
    70518-1197PRAVASTATIN SODIUMPRAVASTATIN SODIUM
    70518-0936Pravastatin SodiumPravastatin Sodium
    70518-1710PRAVASTATIN SODIUMPRAVASTATIN SODIUM

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