FDA.reportPublic FDA data

Ticlopidine Hydrochloride

Product NDC
68151-0079
11-digit product format
681510079
Labeler code
68151
Product ID
68151-0079_c01a9760-cfb9-4d0d-9cf6-12d9deff463f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ticlopidine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Carilion Materials Management
Application
ANDA075149
Marketing category
ANDA
Marketing start
1999-09-07
Marketing end
0000-00-00
Substance
TICLOPIDINE HYDROCHLORIDE
Active strength
250 mg/1
Pharmacologic classes
Decreased Platelet Aggregation [PE],Platelet Aggregation Inhibitor [EPC]
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
02853077-cf58-1b4b-6b29-224747779987Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68151-0079-02020-01-31C16284748780-19d75b9d0-fcfa-f424-e053-dadaa90a57ceTICLOPIDINE HYDROCHLORIDE TABLETS USP 0154 Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68151-0079-0Ticlopidine Hydrochloride1 in 1 BOTTLETABLET, FILM COATED13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TICLOPIDINE HYDROCHLORIDEACTIVE INGREDIENTA1L4914FMFTICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
TICLOPIDINEACTIVE MOIETYOM90ZUW7M1TICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
BUTYLATED HYDROXYANISOLEINACTIVE INGREDIENTREK4960K2UTICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UTICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOTICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30TICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1ATICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
POVIDONESINACTIVE INGREDIENTFZ989GH94ETICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJTICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APTICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPTICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68151-0079TICLOPIDINE HYDROCHLORIDE TABLET, FILM COATED [CARILION MATERIALS MANAGEMENT]3Legacy NDC, 1 package rows20160806_77d619f8-05a3-408a-a6f8-1511694b6a24.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
313406ticlopidine HCl 250 MG Oral TabletPSN77d619f8-05a3-408a-a6f8-1511694b6a243
313406ticlopidine hydrochloride 250 MG Oral TabletSCD77d619f8-05a3-408a-a6f8-1511694b6a243

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
68151-0079-0681510079001 in 1 BOTTLEHistorical