Topiramate

Product NDC
43063-612
11-digit product format
430630612
Labeler code
43063
Product ID
43063-612_de9b258f-a5b3-94e2-e053-2995a90ad858
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Topiramate
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA077627
Marketing category
ANDA
Marketing start
2009-03-27
Marketing end
0000-00-00
Substance
TOPIRAMATE
Active strength
50 mg/1
Pharmacologic classes
Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e5b1b0ba-27f8-4d5d-8943-8aed080fdedcProduct name420260306
6c26dd6d-01b5-4a80-b096-b3a6f7ca6077Product name220250623
cb966f54-bbf0-40fb-b581-80c6648d510cProduct name420250623
6e2fb0d7-40d7-e97c-1375-fa022ff20193Product name420250305
3d272a3f-17c0-421d-bc43-3cbdb719258dProduct name120250303

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43063-612-30EA - Each43063-6126b799a98-3875-4b2a-b25f-914c0f28a0a412015-11-12
43063-612-60EA - Each43063-61232e69e27-0632-4c18-ace6-b6f428a2ead212016-01-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TOPIRAMATEACTIVE INGREDIENT0H73WJJ391TOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
TOPIRAMATEACTIVE MOIETY0H73WJJ391TOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UTOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8TOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
FERRIC OXIDE YELLOWINACTIVE INGREDIENTEX438O2MRTTOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOTOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XTOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30TOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1ATOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8HTOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2TOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJTOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPTOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13
WATERINACTIVE INGREDIENT059QF0KO0RTOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43063-612TOPIRAMATE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]24Legacy NDC20241013_76ae0783-6829-47df-90e4-804313c54041.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
43063-612-304306306123030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-612-30) 2015-10-080000-00-00NoNoCurrent
43063-612-604306306126060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-612-60) 2015-10-080000-00-00NoNoCurrent