Triazolam

Product NDC
21695-303
11-digit product format
216950303
Labeler code
21695
Product ID
21695-303_1da7457b-7225-4950-8108-bbbd8f78f883
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Triazolam
Dosage form
TABLET
Route
ORAL
Labeler
Rebel Distributors Corp
Application
ANDA074224
Marketing category
ANDA
Marketing start
2009-07-13
Marketing end
0000-00-00
Substance
TRIAZOLAM
Active strength
0 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
DEA schedule
CIV
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
50ba0308-e38d-ba7a-26f9-ab61326900c2Product name420240208

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21695-303-102019-09-24C16284748780-1934fe258-4818-48b1-e053-8cdaa90a720aTRIAZOLAM Tablets, USP 0.125 mg and 0.25 mg CIV
21695-303-302019-09-24C16284748780-1934fe258-4818-48b1-e053-8cdaa90a720aTRIAZOLAM Tablets, USP 0.125 mg and 0.25 mg CIV

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21695-303-10Triazolam10 in 1 BOTTLETABLET102
21695-303-30Triazolam30 in 1 BOTTLETABLET302

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-303-10EA - Each21695-303309e9d0e-ff31-4487-aef0-dfcc87617c9512012-07-24
21695-303-30EA - Each21695-30362636f99-01c1-4fcf-896a-fcb4df02e22412012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TRIAZOLAMACTIVE INGREDIENT1HM943223RTRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2
TRIAZOLAMACTIVE MOIETY1HM943223RTRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKTRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UTRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2
DOCUSATE SODIUMINACTIVE INGREDIENTF05Q2T2JA0TRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDTRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30TRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJTRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21695-303TRIAZOLAM TABLET [REBEL DISTRIBUTORS CORP]2Legacy NDC, 2 package rows20111118_73db8a0e-02a9-4613-8feb-e847c965d34f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198317triazolam 0.125 MG Oral TabletPSN73db8a0e-02a9-4613-8feb-e847c965d34f2
198318triazolam 0.25 MG Oral TabletPSN73db8a0e-02a9-4613-8feb-e847c965d34f2
198317triazolam 0.125 MG Oral TabletSCD73db8a0e-02a9-4613-8feb-e847c965d34f2
198318triazolam 0.25 MG Oral TabletSCD73db8a0e-02a9-4613-8feb-e847c965d34f2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
21695-303-102169503031010 in 1 BOTTLEHistorical
21695-303-302169503033030 in 1 BOTTLEHistorical