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"70934-306-30" National Drug Code (NDC)
Alfuzosin Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-306-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)
NDC Code
70934-306-30
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-306-30)
Product NDC
70934-306
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
20190321
Marketing Category Name
ANDA
Application Number
ANDA079057
Manufacturer
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
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/70934-306-30