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"0173-0830-61" National Drug Code (NDC)
Levitra 1 BLISTER PACK in 1 CARTON (0173-0830-61) > 2 TABLET, FILM COATED in 1 BLISTER PACK
(GlaxoSmithKline LLC)
NDC Code
0173-0830-61
Package Description
1 BLISTER PACK in 1 CARTON (0173-0830-61) > 2 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
0173-0830
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Levitra
Non-Proprietary Name
Vardenafil Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20030825
End Marketing Date
20211231
Marketing Category Name
NDA
Application Number
NDA021400
Manufacturer
GlaxoSmithKline LLC
Substance Name
VARDENAFIL HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Phosphodiesterase 5 Inhibitor [EPC],Phosphodiesterase 5 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0173-0830-61