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"60687-736-09" National Drug Code (NDC)
Pantoprazole Sodium 80 BLISTER PACK in 1 CARTON (60687-736-09) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)
(American Health Packaging)
NDC Code
60687-736-09
Package Description
80 BLISTER PACK in 1 CARTON (60687-736-09) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)
Product NDC
60687-736
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pantoprazole Sodium
Non-Proprietary Name
Pantoprazole Sodium
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20230705
Marketing Category Name
ANDA
Application Number
ANDA202038
Manufacturer
American Health Packaging
Substance Name
PANTOPRAZOLE SODIUM
Strength
40
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/60687-736-09