NDC 27241-020

Lansoprazole

Lansoprazole

Lansoprazole is a Oral Capsule, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Ajanta Pharma Limited. The primary component is Lansoprazole.

Product ID27241-020_288d4fd3-ac70-40c5-a7d7-2a1254e4d635
NDC27241-020
Product TypeHuman Prescription Drug
Proprietary NameLansoprazole
Generic NameLansoprazole
Dosage FormCapsule, Delayed Release
Route of AdministrationORAL
Marketing Start Date2016-10-18
Marketing CategoryANDA / ANDA
Application NumberANDA203957
Labeler NameAjanta Pharma Limited
Substance NameLANSOPRAZOLE
Active Ingredient Strength30 mg/1
Pharm ClassesProton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 27241-020-03

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-020-03)
Marketing Start Date2016-10-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 27241-020-50 [27241002050]

Lansoprazole CAPSULE, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA203957
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-10-18

NDC 27241-020-09 [27241002009]

Lansoprazole CAPSULE, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA203957
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-10-18

NDC 27241-020-03 [27241002003]

Lansoprazole CAPSULE, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA203957
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-10-18

NDC 27241-020-10 [27241002010]

Lansoprazole CAPSULE, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA203957
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-10-18

NDC 27241-020-90 [27241002090]

Lansoprazole CAPSULE, DELAYED RELEASE
Marketing CategoryANDA
Application NumberANDA203957
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-10-18

Drug Details

Active Ingredients

IngredientStrength
LANSOPRAZOLE30 mg/1

OpenFDA Data

SPL SET ID:6b9c60e9-b0d2-4aec-a04b-ccc7a62c822b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311277
  • 596843
    • UPC Code
  • 0327241019036
  • 0327241020032

    • Pharmacological Class

    • Proton Pump Inhibitor [EPC]
    • Proton Pump Inhibitors [MoA]
    • Inhibition Gastric Acid Secretion [PE]

    Medicade Reported Pricing

    27241002050 LANSOPRAZOLE DR 30 MG CAPSULE

    Pricing Unit: EA | Drug Type:

    27241002009 LANSOPRAZOLE DR 30 MG CAPSULE

    Pricing Unit: EA | Drug Type:

    27241002003 LANSOPRAZOLE DR 30 MG CAPSULE

    Pricing Unit: EA | Drug Type:

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

    NDCBrand NameGeneric Name
    0093-3008LansoprazoleLansoprazole
    0093-3009LansoprazoleLansoprazole
    0093-7350LansoprazoleLansoprazole
    0093-7351LansoprazoleLansoprazole
    67877-274LansoprazoleLansoprazole
    67877-275LansoprazoleLansoprazole
    68001-111LansoprazoleLansoprazole
    68001-112LansoprazoleLansoprazole
    68016-132LansoprazoleLansoprazole
    68016-756LansoprazoleLansoprazole
    68071-3019lansoprazolelansoprazole
    68071-1972LansoprazoleLansoprazole
    68071-4456LansoprazoleLansoprazole
    68196-019LansoprazoleLansoprazole
    68196-030LansoprazoleLansoprazole
    68382-543lansoprazolelansoprazole
    68382-544lansoprazolelansoprazole
    68382-771LANSOPRAZOLELANSOPRAZOLE
    68382-772LANSOPRAZOLELANSOPRAZOLE
    68788-6390LansoprazoleLansoprazole
    68788-6389LansoprazoleLansoprazole
    68788-7385lansoprazolelansoprazole
    68788-8915LansoprazoleLansoprazole
    68788-9281LansoprazoleLansoprazole
    68788-9269LansoprazoleLansoprazole
    68788-9406LansoprazoleLansoprazole
    68788-8999LansoprazoleLansoprazole
    68788-9677LansoprazoleLansoprazole
    69336-107LANSOPRAZOLELANSOPRAZOLE
    69842-507LansoprazoleLansoprazole
    0591-2448LansoprazoleLansoprazole
    70756-807LansoprazoleLansoprazole
    70771-1132LANSOPRAZOLELANSOPRAZOLE
    70700-262LansoprazoleLansoprazole
    70771-1133LANSOPRAZOLELANSOPRAZOLE
    70700-263LansoprazoleLansoprazole
    70756-806LansoprazoleLansoprazole
    71335-0058LansoprazoleLansoprazole
    71335-0043LansoprazoleLansoprazole
    71335-0660LansoprazoleLansoprazole
    71335-0105lansoprazolelansoprazole
    71335-0917LansoprazoleLansoprazole
    71335-0575lansoprazolelansoprazole
    0781-2148LansoprazoleLansoprazole
    0781-2147LansoprazoleLansoprazole
    0904-6662LansoprazoleLansoprazole
    11822-0117lansoprazolelansoprazole
    21130-019LansoprazoleLansoprazole
    21695-652LansoprazoleLansoprazole
    21695-474LansoprazoleLansoprazole
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.