Primidone

Product NDC
71610-590
11-digit product format
716100590
Labeler code
71610
Product ID
71610-590_a13f7ad0-b9c2-43c3-88cf-f232eacb2140
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Primidone
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA040586
Marketing category
ANDA
Marketing start
2021-02-22
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
Rxcui198150

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
71610-590-60Primidone90 in 1 BOTTLE, PLASTICTABLET901
71610-590-80Primidone180 in 1 BOTTLE, PLASTICTABLET1801
71610-590-92Primidone270 in 1 BOTTLE, PLASTICTABLET2701
71610-590-94Primidone360 in 1 BOTTLE, PLASTICTABLET3601

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71610-590-60EA - Each71610-5903e1489dd-b87a-4d06-af86-e126ba53ba3512021-09-07
71610-590-80EA - Each71610-590510a8e0c-1714-4626-ae35-70af26c5c02812021-09-07
71610-590-92EA - Each71610-59001dfde4c-0dc0-4956-9c4a-9568ed8d2b2512021-09-07
71610-590-94EA - Each71610-5901787bf5c-46e6-4191-be60-64fb053752ef12021-09-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71610-590PRIMIDONE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]1Current NDC, Legacy NDC, 4 package rows20210822_70b93341-ce93-4be5-a782-87c1a26129d7.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198150primidone 50 MG Oral TabletPSN70b93341-ce93-4be5-a782-87c1a26129d71
198150primidone 50 MG Oral TabletSCD70b93341-ce93-4be5-a782-87c1a26129d71

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71610-590-607161005906090 TABLET in 1 BOTTLE, PLASTIC (71610-590-60) 90 tablet2021-08-090000-00-00NoNoCurrent
71610-590-8071610059080180 TABLET in 1 BOTTLE, PLASTIC (71610-590-80) 180 tablet2021-08-090000-00-00NoNoCurrent
71610-590-9271610059092270 TABLET in 1 BOTTLE, PLASTIC (71610-590-92) 270 tablet2021-08-090000-00-00NoNoCurrent
71610-590-9471610059094360 TABLET in 1 BOTTLE, PLASTIC (71610-590-94) 360 tablet2021-08-090000-00-00NoNoCurrent