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"69452-120-20" National Drug Code (NDC)
Oxybutynin Chloride 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69452-120-20)
(Bionpharma Inc.)
NDC Code
69452-120-20
Package Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69452-120-20)
Product NDC
69452-120
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Oxybutynin Chloride
Non-Proprietary Name
Oxybutynin Chloride
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20200316
Marketing Category Name
ANDA
Application Number
ANDA210717
Manufacturer
Bionpharma Inc.
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/69452-120-20