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"72189-132-30" National Drug Code (NDC)
Oxybutynin Chloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)
(DIRECT RX)
NDC Code
72189-132-30
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)
Product NDC
72189-132
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
20200824
Marketing Category Name
ANDA
Application Number
ANDA207138
Manufacturer
DIRECT RX
Substance Name
OXYBUTYNIN CHLORIDE
Strength
10
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/72189-132-30