Metolazone

Product NDC
72162-2390
11-digit product format
721622390
Labeler code
72162
Product ID
72162-2390_2e67d9ca-dbb8-4d25-9046-e535579f3178
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
5 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
METOLAZONE5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiTZ7V40X7VX
Rxcui311671

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
72162-2390-1Metolazone100 in 1 BOTTLETABLET100101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-2390METOLAZONE TABLET [BRYANT RANCH PREPACK]100Current NDC, 1 package rows20240910_7df08bbb-0ab8-485c-8994-48ecadd096f1.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311671metOLazone 5 MG Oral TabletPSN7df08bbb-0ab8-485c-8994-48ecadd096f1101
311671metolazone 5 MG Oral TabletSCD7df08bbb-0ab8-485c-8994-48ecadd096f1101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-2390-172162239001100 TABLET in 1 BOTTLE (72162-2390-1) 100 tablet2024-06-15NoNoHistorical