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"72888-032-05" National Drug Code (NDC)
Oxybutynin Chloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-032-05)
(Advagen Pharma Limited)
NDC Code
72888-032-05
Package Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72888-032-05)
Product NDC
72888-032
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Oxybutynin Chloride
Non-Proprietary Name
Oxybutynin Chloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20201027
Marketing Category Name
ANDA
Application Number
ANDA214415
Manufacturer
Advagen Pharma Limited
Substance Name
OXYBUTYNIN CHLORIDE
Strength
15
Strength Unit
mg/1
Pharmacy Classes
Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72888-032-05