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"51655-967-52" National Drug Code (NDC)
Alfuzosin Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-967-52)
(Northwind Pharmaceuticals, LLC)
NDC Code
51655-967-52
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-967-52)
Product NDC
51655-967
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
20230629
Marketing Category Name
ANDA
Application Number
ANDA203192
Manufacturer
Northwind Pharmaceuticals, LLC
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/51655-967-52