Metolazone

Product NDC
72162-2391
11-digit product format
721622391
Labeler code
72162
Product ID
72162-2391_d7f7188f-a5fd-4258-b655-47a3e35a7d1e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metolazone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA213827
Marketing category
ANDA
Marketing start
2024-06-15
Substance
METOLAZONE
Active strength
10 mg/1
Pharmacologic classes
Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Metolazone
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METOLAZONE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiTZ7V40X7VX
Rxcui197978

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4e48c581-6027-290d-65f0-1b09c39dc1e8Product name620250625

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-2391-1Metolazone100 in 1 BOTTLETABLET100101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-2391METOLAZONE TABLET [BRYANT RANCH PREPACK]100Current NDC, 1 package rows20240910_27ab833e-b809-4a80-b7fc-b3599f1751d3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197978metOLazone 10 MG Oral TabletPSN27ab833e-b809-4a80-b7fc-b3599f1751d3101
197978metolazone 10 MG Oral TabletSCD27ab833e-b809-4a80-b7fc-b3599f1751d3101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-2391-172162239101100 TABLET in 1 BOTTLE (72162-2391-1) 100 tablet2024-06-15NoNoCurrent