NDC 71335-0105

lansoprazole

Lansoprazole

lansoprazole is a Oral Capsule, Delayed Release Pellets in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Lansoprazole.

Product ID71335-0105_354b4e3f-9cec-43d0-b889-f2882a8af188
NDC71335-0105
Product TypeHuman Prescription Drug
Proprietary Namelansoprazole
Generic NameLansoprazole
Dosage FormCapsule, Delayed Release Pellets
Route of AdministrationORAL
Marketing Start Date2013-08-23
Marketing CategoryANDA / ANDA
Application NumberANDA202366
Labeler NameBryant Ranch Prepack
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 Through2019-12-31

Packaging

NDC 71335-0105-1

56 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0105-1)
Marketing Start Date2013-08-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0105-3 [71335010503]

lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA202366
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-23

NDC 71335-0105-1 [71335010501]

lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA202366
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-23

NDC 71335-0105-6 [71335010506]

lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA202366
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-23

NDC 71335-0105-4 [71335010504]

lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA202366
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-23

NDC 71335-0105-2 [71335010502]

lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA202366
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-23

NDC 71335-0105-5 [71335010505]

lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA202366
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-23

NDC 71335-0105-7 [71335010507]

lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA202366
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-08-23

Drug Details

Active Ingredients

IngredientStrength
LANSOPRAZOLE30 mg/1

OpenFDA Data

SPL SET ID:67d6f7fb-7347-4fa8-9a4e-5dd748ce3ddd
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311277

    • Pharmacological Class

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

    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.