Primidone

Product NDC
55111-477
11-digit product format
551110477
Labeler code
55111
Product ID
55111-477_6f5c36d3-3f99-803c-5be6-66b2e1058946
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Primidone
Dosage form
TABLET
Route
ORAL
Labeler
Dr. Reddy's Laboratories Limited
Application
ANDA040862
Marketing category
ANDA
Marketing start
2008-10-03
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
55111-477-01Primidone100 in 1 BOTTLETABLET1003
55111-477-05Primidone500 in 1 BOTTLETABLET5003
55111-477-30Primidone30 in 1 BOTTLETABLET303
55111-477-60Primidone60 in 1 BOTTLETABLET603
55111-477-78Primidone10 in 1 CARTONTABLET103
55111-477-79Primidone10 in 1 BLISTER PACKTABLET103

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55111-477-01EA - Each55111-4773fd1ea19-94c9-401f-98b6-012c9eee6a1212012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
primidoneACTIVE INGREDIENT13AFD7670QPRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2
primidoneACTIVE MOIETY13AFD7670QPRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2
ferric oxide yellowINACTIVE INGREDIENTEX438O2MRTPRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2
lactose monohydrateINACTIVE INGREDIENTEWQ57Q8I5XPRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2
magnesium stearateINACTIVE INGREDIENT70097M6I30PRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2
sodium lauryl sulfateINACTIVE INGREDIENT368GB5141JPRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2
sodium starch glycolate type A potatoINACTIVE INGREDIENT5856J3G2A2PRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2
talcINACTIVE INGREDIENT7SEV7J4R1UPRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2
waterINACTIVE INGREDIENT059QF0KO0RPRIMIDONE TABLET [DR. REDDY'S LABORATORIES LTD]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55111-477PRIMIDONE TABLET [DR. REDDY'S LABORATORIES LIMITED]3Current NDC, Legacy NDC, 6 package rows20171206_a4f917f4-2aa2-c3ed-071e-232fa0f125e8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
96304primidone 250 MG Oral TabletPSNa4f917f4-2aa2-c3ed-071e-232fa0f125e83
198150primidone 50 MG Oral TabletPSNa4f917f4-2aa2-c3ed-071e-232fa0f125e83
96304primidone 250 MG Oral TabletSCDa4f917f4-2aa2-c3ed-071e-232fa0f125e83
198150primidone 50 MG Oral TabletSCDa4f917f4-2aa2-c3ed-071e-232fa0f125e83

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55111-477-0155111047701100 TABLET in 1 BOTTLE (55111-477-01) 100 tablet2008-10-030000-00-00NoNoCurrent
55111-477-0555111047705500 TABLET in 1 BOTTLE (55111-477-05) 500 tablet2008-10-030000-00-00NoNoCurrent
55111-477-305511104773030 TABLET in 1 BOTTLE (55111-477-30) 30 tablet2008-10-030000-00-00NoNoCurrent
55111-477-605511104776060 TABLET in 1 BOTTLE (55111-477-60) 60 tablet2008-10-030000-00-00NoNoCurrent
55111-477-785511104777810 BLISTER PACK in 1 CARTON (55111-477-78) / 10 TABLET in 1 BLISTER PACK (55111-477-79) 10 blister pack2008-10-030000-00-00NoNoCurrent
55111-477-795511104777910 in 1 BLISTER PACKHistorical