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"49035-739-33" National Drug Code (NDC)
Lansoprazole 3 BOTTLE in 1 PACKAGE, COMBINATION (49035-739-33) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49035-739-52)
(Wal-Mart Stores Inc)
NDC Code
49035-739-33
Package Description
3 BOTTLE in 1 PACKAGE, COMBINATION (49035-739-33) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49035-739-52)
Product NDC
49035-739
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Lansoprazole
Non-Proprietary Name
Lansoprazole
Dosage Form
CAPSULE, DELAYED RELEASE
Usage
ORAL
Start Marketing Date
20120518
Marketing Category Name
ANDA
Application Number
ANDA202194
Manufacturer
Wal-Mart Stores Inc
Substance Name
LANSOPRAZOLE
Strength
15
Strength Unit
mg/1
Pharmacy Classes
Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49035-739-33