Metolazone

Product NDC
0904-7520
11-digit product format
009047520
Labeler code
0904
Product ID
0904-7520_89201e19-d0e8-4192-b2a1-150e9d2c104d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metolazone
Dosage form
TABLET
Route
ORAL
Labeler
Major Pharmaceuticals
Application
ANDA215616
Marketing category
ANDA
Marketing start
2025-11-20
Substance
METOLAZONE
Active strength
2.5 mg/1
Pharmacologic classes
Increased Diuresis [PE], Thiazide-like Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Metolazone
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METOLAZONE2.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiTZ7V40X7VX
Rxcui197979, 311671

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
0904-7520-61Metolazone100 in 1 CARTONTABLET1001
0904-7520-61Metolazone1 in 1 BLISTER PACKTABLET11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197979metOLazone 2.5 MG Oral TabletPSN89201e19-d0e8-4192-b2a1-150e9d2c104d1
311671metOLazone 5 MG Oral TabletPSN89201e19-d0e8-4192-b2a1-150e9d2c104d1
197979metolazone 2.5 MG Oral TabletSCD89201e19-d0e8-4192-b2a1-150e9d2c104d1
311671metolazone 5 MG Oral TabletSCD89201e19-d0e8-4192-b2a1-150e9d2c104d1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0904-7520-6100904752061100 BLISTER PACK in 1 CARTON (0904-7520-61) / 1 TABLET in 1 BLISTER PACK100 blister pack2025-11-20NoNoCurrent