FDA.reportPublic FDA data

Terbinafine

Product NDC
50090-3654
11-digit product format
500903654
Labeler code
50090
Product ID
50090-3654_96cc504c-9106-48d2-a614-81ad3a4e977c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Terbinafine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078297
Marketing category
ANDA
Marketing start
2007-07-02
Substance
TERBINAFINE HYDROCHLORIDE
Active strength
250 mg/1
Pharmacologic classes
Allylamine Antifungal [EPC], Allylamine [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
TERBINAFINE HYDROCHLORIDE250 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii012C11ZU6G
Rxcui313222

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
55a24767-1759-5f6a-8888-ea4aa0adac21Product name120140508
db9701af-cb4f-b8ba-d282-6bc5b6b7c467Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-3654-02024-05-22C16284748780-1f386c649-e863-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use TERBINAFINE TABLETS safely and effectively. See full prescribing information for TERBINAFINE TABLETS. TERBINAFINE tablets, for oral use Initial U.S. Approval: 1992
50090-3654-12024-05-22C16284748780-1f386c649-e863-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use TERBINAFINE TABLETS safely and effectively. See full prescribing information for TERBINAFINE TABLETS. TERBINAFINE tablets, for oral use Initial U.S. Approval: 1992
50090-3654-02023-01-30C16284748780-1f386c649-e863-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use TERBINAFINE TABLETS safely and effectively. See full prescribing information for TERBINAFINE TABLETS. TERBINAFINE tablets, for oral use Initial U.S. Approval: 1992
50090-3654-12023-01-30C16284748780-1f386c649-e863-0266-e053-dadaa90a7c1aThese highlights do not include all the information needed to use TERBINAFINE TABLETS safely and effectively. See full prescribing information for TERBINAFINE TABLETS. TERBINAFINE tablets, for oral use Initial U.S. Approval: 1992

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-3654-0Terbinafine30 in 1 BOTTLE, PLASTICTABLET307
50090-3654-1Terbinafine90 in 1 BOTTLETABLET907

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-3654-0EA - Each50090-365498fa9233-1f4b-493a-a4da-9627a8bde0e412024-06-10
50090-3654-1EA - Each50090-3654b35d00ec-8f0d-4024-ae0d-c2b299968e1112024-06-10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-3654TERBINAFINE (TERBINAFINE HYDROCHLORIDE) TABLET [A-S MEDICATION SOLUTIONS]7Current NDC, Legacy NDC, 2 package rows20240524_79a39fb1-12b7-4b1e-9f28-102af34d0459.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313222terbinafine HCl 250 MG Oral TabletPSN79a39fb1-12b7-4b1e-9f28-102af34d04597
313222terbinafine 250 MG Oral TabletSCD79a39fb1-12b7-4b1e-9f28-102af34d04597
313222terbinafine (as terbinafine HCl) 250 MG Oral TabletSY79a39fb1-12b7-4b1e-9f28-102af34d04597

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-3654-05009036540030 TABLET in 1 BOTTLE, PLASTIC (50090-3654-0) 30 tablet2014-11-280000-00-00NoNoCurrent
50090-3654-15009036540190 TABLET in 1 BOTTLE (50090-3654-1) 90 tablet2018-10-110000-00-00NoNoCurrent