NDC 62175-430

Lansoprazole

Lansoprazole

Lansoprazole is a Oral Capsule, Delayed Release Pellets in the Human Prescription Drug category. It is labeled and distributed by Lannett Company, Inc.. The primary component is Lansoprazole.

Product ID62175-430_03c24721-9782-4090-9d8d-5517b3e7cbc9
NDC62175-430
Product TypeHuman Prescription Drug
Proprietary NameLansoprazole
Generic NameLansoprazole
Dosage FormCapsule, Delayed Release Pellets
Route of AdministrationORAL
Marketing Start Date2017-09-28
Marketing CategoryANDA / ANDA
Application NumberANDA207156
Labeler NameLannett Company, Inc.
Substance NameLANSOPRAZOLE
Active Ingredient Strength30 mg/1
Pharm ClassesInhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 62175-430-32

30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (62175-430-32)
Marketing Start Date2017-09-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62175-430-37 [62175043037]

Lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA207156
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 62175-430-32 [62175043032]

Lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA207156
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-09-28

NDC 62175-430-43 [62175043043]

Lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA207156
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-28

NDC 62175-430-46 [62175043046]

Lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA207156
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-09-28

NDC 62175-430-41 [62175043041]

Lansoprazole CAPSULE, DELAYED RELEASE PELLETS
Marketing CategoryANDA
Application NumberANDA207156
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-09-28

Drug Details

Active Ingredients

IngredientStrength
LANSOPRAZOLE30 mg/1

OpenFDA Data

SPL SET ID:11c323ff-3aeb-453f-b9e2-5baa51d8cf50
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311277
  • 596843
    • UPC Code
  • 0362175415325
  • 0362175430328

    • Pharmacological Class

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