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"51079-722-20" National Drug Code (NDC)
Oxybutynin Chloride 100 BLISTER PACK in 1 CARTON (51079-722-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-722-01)
(Mylan Institutional Inc.)
NDC Code
51079-722-20
Package Description
100 BLISTER PACK in 1 CARTON (51079-722-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-722-01)
Product NDC
51079-722
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
20061127
Marketing Category Name
ANDA
Application Number
ANDA076702
Manufacturer
Mylan Institutional Inc.
Substance Name
OXYBUTYNIN CHLORIDE
Strength
5
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/51079-722-20