NDC 24658-260

Gemfibrozil

Gemfibrozil

Gemfibrozil is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Puracap Laboratories Llc Dba Blu Pharmaceuticals. The primary component is Gemfibrozil.

Product ID24658-260_2e4778c2-dd55-4eae-872f-449cc71980b6
NDC24658-260
Product TypeHuman Prescription Drug
Proprietary NameGemfibrozil
Generic NameGemfibrozil
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2011-04-01
Marketing CategoryANDA / ANDA
Application NumberANDA078012
Labeler NamePuraCap Laboratories LLC dba Blu Pharmaceuticals
Substance NameGEMFIBROZIL
Active Ingredient Strength600 mg/1
Pharm ClassesPeroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 24658-260-05

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24658-260-05)
Marketing Start Date2011-04-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 24658-260-18 [24658026018]

Gemfibrozil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078012
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-04-01

NDC 24658-260-60 [24658026060]

Gemfibrozil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078012
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-04-01

NDC 24658-260-05 [24658026005]

Gemfibrozil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078012
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-04-01

NDC 24658-260-30 [24658026030]

Gemfibrozil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078012
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-04-01

NDC 24658-260-90 [24658026090]

Gemfibrozil TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078012
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-04-01

Drug Details

Active Ingredients

IngredientStrength
GEMFIBROZIL600 mg/1

OpenFDA Data

SPL SET ID:fdcee21a-097d-4354-bc91-e92cfdffac62
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310459
    • UPC Code
  • 0324658260600

    • Pharmacological Class

    • Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]
    • PPAR alpha [CS]
    • Peroxisome Proliferator Receptor alpha Agonist [EPC]
    • Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]
    • PPAR alpha [CS]
    • Peroxisome Proliferator Receptor alpha Agonist [EPC]

    Medicade Reported Pricing

    24658026090 GEMFIBROZIL 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    24658026060 GEMFIBROZIL 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    24658026018 GEMFIBROZIL 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    24658026005 GEMFIBROZIL 600 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Gemfibrozil" or generic name "Gemfibrozil"

    NDCBrand NameGeneric Name
    0093-0670GemfibrozilGemfibrozil
    0143-9130GemfibrozilGemfibrozil
    0143-9707GemfibrozilGemfibrozil
    0179-0221GemfibrozilGemfibrozil
    0615-3559GemfibrozilGemfibrozil
    0615-8354GemfibrozilGemfibrozil
    10544-569GemfibrozilGemfibrozil
    16571-784GemfibrozilGemfibrozil
    16714-101Gemfibrozilgemfibrozil
    21695-732GemfibrozilGemfibrozil
    24658-260GemfibrozilGemfibrozil
    31722-128GEMFIBROZILGemfibrozil
    31722-225GemfibrozilGemfibrozil
    33261-146GemfibrozilGemfibrozil
    42806-260GEMFIBROZILGEMFIBROZIL
    43063-745GemfibrozilGemfibrozil
    43063-921GEMFIBROZILGEMFIBROZIL
    43353-090GemfibrozilGemfibrozil
    43353-772GemfibrozilGemfibrozil
    43602-452GEMFIBROZILGemfibrozil
    50090-0458GemfibrozilGemfibrozil
    50090-2450GemfibrozilGemfibrozil
    50090-2902GemfibrozilGemfibrozil
    50090-5808GEMFIBROZILGemfibrozil
    50268-350GemfibrozilGemfibrozil
    68071-1733GemfibrozilGemfibrozil
    68071-4053GEMFIBROZILGEMFIBROZIL
    68071-4011GEMFIBROZILGEMFIBROZIL
    68071-4631GemfibrozilGemfibrozil
    68071-4421GemfibrozilGemfibrozil
    68151-2893GemfibrozilGemfibrozil
    68382-553GemfibrozilGemfibrozil
    68788-6447GemfibrozilGemfibrozil
    68788-7011GEMFIBROZILGEMFIBROZIL
    68788-9149GemfibrozilGemfibrozil
    69097-821GemfibrozilGemfibrozil
    70518-1563GemfibrozilGemfibrozil
    70518-1301GemfibrozilGemfibrozil
    70771-1431GemfibrozilGemfibrozil
    71205-169GemfibrozilGemfibrozil
    71209-008GemfibrozilGemfibrozil
    71335-0051GEMFIBROZILGEMFIBROZIL
    71335-0971GemfibrozilGemfibrozil
    71335-0899GemfibrozilGemfibrozil
    71335-0515GemfibrozilGemfibrozil
    71610-200GemfibrozilGemfibrozil
    71610-107GemfibrozilGemfibrozil
    75834-131GemfibrozilGemfibrozil
    76282-225GemfibrozilGemfibrozil
    50436-6540GemfibrozilGemfibrozil
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.