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"49349-923-38" National Drug Code (NDC)
Hydrochlorothiazide 3 TABLET in 1 BLISTER PACK (49349-923-38)
(REMEDYREPACK INC.)
NDC Code
49349-923-38
Package Description
3 TABLET in 1 BLISTER PACK (49349-923-38)
Product NDC
49349-923
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hydrochlorothiazide
Non-Proprietary Name
Hydrochlorothiazide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20120315
Marketing Category Name
ANDA
Application Number
ANDA040412
Manufacturer
REMEDYREPACK INC.
Substance Name
HYDROCHLOROTHIAZIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-923-38