Home NDC 64125-131 Hydrochlorothiazide
Product NDC 64125-131
11-digit product format 641250131
Labeler code 64125
Product ID 64125-131_85594a90-366d-4d66-8d80-218dffef94d8
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Hydrochlorothiazide
Dosage form TABLET
Route ORAL
Labeler Excellium Pharmaceutical Inc.
Application ANDA040702
Marketing category ANDA
Marketing start 2007-06-01
Marketing end 0000-00-00
Substance HYDROCHLOROTHIAZIDE
Active strength 25 mg/1
Pharmacologic classes Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
NDC exclude flag E
Listing certified through 2017-12-31
Current FDA listing Historical FDA.report record DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64125-131-01 Hydrochlorothiazide 100 in 1 BOTTLE TABLET 100 2 64125-131-10 Hydrochlorothiazide 1000 in 1 BOTTLE TABLET 1000 2 64125-131-50 Hydrochlorothiazide 5000 in 1 BOTTLE TABLET 5000 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64125-131 HYDROCHLOROTHIAZIDE TABLET [EXCELLIUM PHARMACEUTICAL INC.] 2 Legacy NDC, 3 package rows 20120905_4ca95d04-765a-47a8-8118-48c7740f4e81.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 64125-131-01 64125013101 100 in 1 BOTTLE Historical 64125-131-10 64125013110 1000 in 1 BOTTLE Historical 64125-131-50 64125013150 5000 in 1 BOTTLE Historical