Primidone

Product NDC
65162-544
11-digit product format
651620544
Labeler code
65162
Product ID
65162-544_fe35e838-40df-42c2-bcbf-0ed9aa7eaa5b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Primidone
Dosage form
TABLET
Route
ORAL
Labeler
Amneal Pharmaceuticals LLC
Application
ANDA040866
Marketing category
ANDA
Marketing start
2009-12-24
Substance
PRIMIDONE
Active strength
50 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PRIMIDONE50 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii13AFD7670Q
Rxcui96304, 198150

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3a6e0ba9-1dda-c47a-a8e3-5844e445a4f8Product name320250114

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65162-544-10Primidone100 in 1 BOTTLETABLET10022
65162-544-11Primidone1000 in 1 BOTTLETABLET100022
65162-544-50Primidone500 in 1 BOTTLETABLET50022

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65162-544-10EA - Each65162-544cfb4059f-f4a8-41bd-98c7-c92788e0998d12012-07-24
65162-544-50EA - Each65162-54489fb70e7-de4f-43f5-b1f0-3d540fcb713712012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PRIMIDONEACTIVE INGREDIENT13AFD7670QPRIMIDONE TABLET [AMNEAL PHARMACEUTICALS]10
PRIMIDONEACTIVE MOIETY13AFD7670QPRIMIDONE TABLET [AMNEAL PHARMACEUTICALS]10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65162-544PRIMIDONE TABLET [AMNEAL PHARMACEUTICALS LLC]22Current NDC, Legacy NDC, 3 package rows20241031_02ba0182-0870-4c0d-a814-a1dc427d47b8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
96304primidone 250 MG Oral TabletPSN02ba0182-0870-4c0d-a814-a1dc427d47b822
198150primidone 50 MG Oral TabletPSN02ba0182-0870-4c0d-a814-a1dc427d47b822
96304primidone 250 MG Oral TabletSCD02ba0182-0870-4c0d-a814-a1dc427d47b822
198150primidone 50 MG Oral TabletSCD02ba0182-0870-4c0d-a814-a1dc427d47b822

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
65162-544-1065162054410100 TABLET in 1 BOTTLE (65162-544-10) 100 tablet2009-12-240000-00-00NoNoCurrent
65162-544-11651620544111000 TABLET in 1 BOTTLE (65162-544-11) 1000 tablet2009-12-240000-00-00NoNoCurrent
65162-544-5065162054450500 TABLET in 1 BOTTLE (65162-544-50) 500 tablet2009-12-240000-00-00NoNoCurrent