FDA.reportPublic FDA data

NDC 67296-1487 - Hydrochlorothiazide

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
67296-1487
Package NDCs from labels
67296-1487-3
Manufacturer
Redpharm Drug, Inc. | Prinston Pharmaceutical Inc. | Redpharm Drug, Inc
Effective date
2024-08-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
HYDROCHLOROTHIAZIDE TABLETS, USP 25 mg and 50 mgRedpharm Drug, Inc. | Prinston Pharmaceutical Inc. | Redpharm Drug, Inc2024-08-08HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67296-1487-3Hydrochlorothiazide30 in 1 BOTTLE, PLASTICTABLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67296-1487HYDROCHLOROTHIAZIDE TABLET [REDPHARM DRUG, INC.]21 package rows20240809_f3d2d017-e6a0-4823-e053-2995a90a5764.zip