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"52125-022-02" National Drug Code (NDC)
Oxybutynin Chloride 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-022-02)
(REMEDYREPACK INC.)
NDC Code
52125-022-02
Package Description
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-022-02)
Product NDC
52125-022
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
20130225
Marketing Category Name
ANDA
Application Number
ANDA076745
Manufacturer
REMEDYREPACK 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/52125-022-02