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"70518-2666-2" National Drug Code (NDC)
Hydrochlorothiazide 90 TABLET in 1 BOTTLE, PLASTIC (70518-2666-2)
(REMEDYREPACK INC.)
NDC Code
70518-2666-2
Package Description
90 TABLET in 1 BOTTLE, PLASTIC (70518-2666-2)
Product NDC
70518-2666
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hydrochlorothiazide
Non-Proprietary Name
Hydrochlorothiazide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200331
Marketing Category Name
ANDA
Application Number
ANDA040702
Manufacturer
REMEDYREPACK INC.
Substance Name
HYDROCHLOROTHIAZIDE
Strength
12.5
Strength Unit
mg/1
Pharmacy Classes
Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2666-2