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"55111-332-78" National Drug Code (NDC)
Pantoprazole 10 BLISTER PACK in 1 CARTON (55111-332-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-332-79)
(Dr.Reddy's Laboratories Limited)
NDC Code
55111-332-78
Package Description
10 BLISTER PACK in 1 CARTON (55111-332-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-332-79)
Product NDC
55111-332
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pantoprazole
Non-Proprietary Name
Pantoprazole
Dosage Form
TABLET, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20110119
Marketing Category Name
ANDA
Application Number
ANDA077619
Manufacturer
Dr.Reddy's Laboratories Limited
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/55111-332-78