BUSPIRONE HYDROCHLORIDE

Product NDC
58517-340
11-digit product format
585170340
Labeler code
58517
Product ID
58517-340_5cbda603-31ef-43b8-a650-015822a1e2aa
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
BUSPIRONE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
New Horizon Rx Group, LLC
Application
ANDA074253
Marketing category
ANDA
Marketing start
2013-08-25
Marketing end
0000-00-00
Substance
BUSPIRONE HYDROCHLORIDE
Active strength
10 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a9968269-ddf2-400e-9170-7376dcf3545aProduct name120251215
2cf3c2e9-d566-c982-009a-188fe4f776b9Product name820200428
4a9096ce-7b98-89e5-5942-15f48c4f7abfProduct name520190711

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58517-340-302019-11-27C16284748780-19855e2a2-4a94-60a7-e053-dbdaa90a05bdBuspirone Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58517-340-30BUSPIRONE HYDROCHLORIDE30 in 1 BOTTLETABLET302

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58517-340-30EA - Each58517-34034b1d652-41a6-4740-a9de-068cb96c069612013-11-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BUSPIRONE HYDROCHLORIDEACTIVE INGREDIENT207LT9J9OCBUSPIRONE HYDROCHLORIDE TABLET [NEW HORIZON RX GROUP, LLC]2
BUSPIRONEACTIVE MOIETYTK65WKS8HLBUSPIRONE HYDROCHLORIDE TABLET [NEW HORIZON RX GROUP, LLC]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UBUSPIRONE HYDROCHLORIDE TABLET [NEW HORIZON RX GROUP, LLC]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XBUSPIRONE HYDROCHLORIDE TABLET [NEW HORIZON RX GROUP, LLC]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30BUSPIRONE HYDROCHLORIDE TABLET [NEW HORIZON RX GROUP, LLC]2
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4BUSPIRONE HYDROCHLORIDE TABLET [NEW HORIZON RX GROUP, LLC]2
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2BUSPIRONE HYDROCHLORIDE TABLET [NEW HORIZON RX GROUP, LLC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58517-340BUSPIRONE HYDROCHLORIDE TABLET [NEW HORIZON RX GROUP, LLC]2Legacy NDC, 1 package rows20140101_2ae6f5c5-8069-4113-b06b-1e7f2846ed6d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
866083busPIRone HCl 10 MG Oral TabletPSN2ae6f5c5-8069-4113-b06b-1e7f2846ed6d2
866083buspirone hydrochloride 10 MG Oral TabletSCD2ae6f5c5-8069-4113-b06b-1e7f2846ed6d2
866083buspirone HCl 10 MG (buspirone 9.1 MG) Oral TabletSY2ae6f5c5-8069-4113-b06b-1e7f2846ed6d2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
58517-340-305851703403030 in 1 BOTTLEHistorical