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"69367-123-07" National Drug Code (NDC)
Hydrochlorothiazide 1000 mg in 1 BOTTLE (69367-123-07)
(Westminster Pharmaceuticals, LLC)
NDC Code
69367-123-07
Package Description
1000 mg in 1 BOTTLE (69367-123-07)
Product NDC
69367-123
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hydrochlorothiazide
Non-Proprietary Name
Hydrochlorothiazide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160201
Marketing Category Name
ANDA
Application Number
ANDA203018
Manufacturer
Westminster Pharmaceuticals, LLC
Substance Name
HYDROCHLOROTHIAZIDE
Strength
50
Strength Unit
mg/50mg
Pharmacy Classes
Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69367-123-07