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"69097-844-12" National Drug Code (NDC)
Alfuzosin Hydrochloride 500 TABLET in 1 BOTTLE (69097-844-12)
(Cipla USA Inc.)
NDC Code
69097-844-12
Package Description
500 TABLET in 1 BOTTLE (69097-844-12)
Product NDC
69097-844
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Alfuzosin Hydrochloride
Proprietary Name Suffix
Extended Release
Non-Proprietary Name
Alfuzosin Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160630
Marketing Category Name
ANDA
Application Number
ANDA090284
Manufacturer
Cipla USA Inc.
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/69097-844-12