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"63629-2353-1" National Drug Code (NDC)
Alfuzosin Hydrochloride 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2353-1)
(Bryant Ranch Prepack)
NDC Code
63629-2353-1
Package Description
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2353-1)
Product NDC
63629-2353
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Alfuzosin Hydrochloride
Non-Proprietary Name
Alfuzosin Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20111122
End Marketing Date
20240831
Marketing Category Name
ANDA
Application Number
ANDA079057
Manufacturer
Bryant Ranch Prepack
Substance Name
ALFUZOSIN HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63629-2353-1