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"70756-018-51" National Drug Code (NDC)
Pantoprazole Sodium Delayed-release 500 TABLET in 1 BOTTLE (70756-018-51)
(Lifestar Pharma LLC)
NDC Code
70756-018-51
Package Description
500 TABLET in 1 BOTTLE (70756-018-51)
Product NDC
70756-018
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pantoprazole Sodium Delayed-release
Non-Proprietary Name
Pantoprazole Sodium Delayed-release
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20240425
Marketing Category Name
ANDA
Application Number
ANDA215880
Manufacturer
Lifestar Pharma LLC
Substance Name
PANTOPRAZOLE SODIUM
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70756-018-51