Exemestane

Product NDC
70771-1374
11-digit product format
707711374
Labeler code
70771
Product ID
70771-1374_7892e262-ddad-4e1d-909d-d8590bb082de
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Exemestane
Dosage form
TABLET
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA202602
Marketing category
ANDA
Marketing start
2018-10-08
Substance
EXEMESTANE
Active strength
25 mg/1
Pharmacologic classes
Aromatase Inhibitor [EPC], Aromatase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EXEMESTANE25 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiNY22HMQ4BX
Rxcui310261

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1fe6d34b-d50f-eeb9-bd0c-3f0d6b635985Product name920230126

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70771-1374-3Exemestane30 in 1 BOTTLETABLET306

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70771-1374EXEMESTANE TABLET [ZYDUS LIFESCIENCES LIMITED]6Current NDC, Legacy NDC, 1 package rows20241201_fab5468a-d5b7-45e3-b8b2-ed902fddd3a6.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310261exemestane 25 MG Oral TabletPSNfab5468a-d5b7-45e3-b8b2-ed902fddd3a66
310261exemestane 25 MG Oral TabletSCDfab5468a-d5b7-45e3-b8b2-ed902fddd3a66

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70771-1374-37077113740330 TABLET in 1 BOTTLE (70771-1374-3) 30 tablet2018-10-080000-00-00NoNoCurrent