Citalopram

Product NDC
64205-207
11-digit product format
642050207
Labeler code
64205
Product ID
64205-207_1b3a8591-6566-4561-93da-6d3d5db1c4b5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Citalopram
Dosage form
TABLET
Route
ORAL
Labeler
ReadyMeds
Application
ANDA077534
Marketing category
ANDA
Marketing start
2011-01-01
Marketing end
0000-00-00
Substance
CITALOPRAM HYDROBROMIDE
Active strength
20 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
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
475812f9-1b2c-4cb0-9e72-1e52f935ae6fProduct name120221114
0b05d650-9b7b-4b36-a6f4-1a850d5a2e64Product name120151228
e61ea6cb-0b08-40a9-a984-7b23201c7aa2Product name120151222

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64205-207-302019-11-27C16284748780-19855e2a2-3966-60a7-e053-dbdaa90a05bdCitalopram Tablets, USP Rx Only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64205-207-30Citalopram30 in 1 BOTTLETABLET305

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CITALOPRAM HYDROBROMIDEACTIVE INGREDIENTI1E9D14F36CITALOPRAM TABLET [READYMEDS]5
CITALOPRAMACTIVE MOIETY0DHU5B8D6VCITALOPRAM TABLET [READYMEDS]5
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UCITALOPRAM TABLET [READYMEDS]5
COPOVIDONEINACTIVE INGREDIENTD9C330MD8BCITALOPRAM TABLET [READYMEDS]5
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48CITALOPRAM TABLET [READYMEDS]5
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G675CITALOPRAM TABLET [READYMEDS]5
HYPROMELLOSE 2910 (6 MPA.S)INACTIVE INGREDIENT0WZ8WG20P6CITALOPRAM TABLET [READYMEDS]5
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XCITALOPRAM TABLET [READYMEDS]5
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30CITALOPRAM TABLET [READYMEDS]5
POLYETHYLENE GLYCOL 400INACTIVE INGREDIENTB697894SGQCITALOPRAM TABLET [READYMEDS]5
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPCITALOPRAM TABLET [READYMEDS]5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64205-207CITALOPRAM TABLET [READYMEDS]5Legacy NDC, 1 package rows20140501_aeea4b3f-6878-4211-a85a-b2a62772b3f8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
200371citalopram 20 MG Oral TabletPSNaeea4b3f-6878-4211-a85a-b2a62772b3f85
200371citalopram 20 MG Oral TabletSCDaeea4b3f-6878-4211-a85a-b2a62772b3f85
200371citalopram 20 MG (as citalopram HBr 24.99 MG) Oral TabletSYaeea4b3f-6878-4211-a85a-b2a62772b3f85

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
64205-207-306420502073030 in 1 BOTTLEHistorical