Citalopram

Product NDC
51655-680
11-digit product format
516550680
Labeler code
51655
Product ID
51655-680_4950c3d6-8a7b-8e8f-e063-6294a90a015c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Citalopram Hydrobromide
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Northwind Health Company, LLC
Application
ANDA077031
Marketing category
ANDA
Marketing start
2022-03-02
Substance
CITALOPRAM HYDROBROMIDE
Active strength
20 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Citalopram
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CITALOPRAM HYDROBROMIDE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiI1E9D14F36
Rxcui200371

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51655-680-26Citalopram90 in 1 BOTTLE, PLASTICTABLET, FILM COATED903
51655-680-52Citalopram30 in 1 BOTTLE, PLASTICTABLET, FILM COATED303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-680CITALOPRAM (CITALOPRAM HYDROBROMIDE) TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]2Current NDC, 2 package rows20240727_d9ccb3fb-b607-9491-e053-2995a90a39c9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
200371citalopram 20 MG Oral TabletPSNd9ccb3fb-b607-9491-e053-2995a90a39c93
200371citalopram 20 MG Oral TabletSCDd9ccb3fb-b607-9491-e053-2995a90a39c93
200371citalopram 20 MG (as citalopram HBr 24.99 MG) Oral TabletSYd9ccb3fb-b607-9491-e053-2995a90a39c93

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
51655-680-265165506802690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-26) 2022-05-04NoNoCurrent
51655-680-525165506805230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-680-52) 2022-03-02NoNoCurrent