Citalopram Hydrobromide

Product NDC
70934-090
11-digit product format
709340090
Labeler code
70934
Product ID
70934-090_b97fa670-62d5-5b2d-e053-2a95a90ac227
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Citalopram Hydrobromide
Dosage form
TABLET
Route
ORAL
Labeler
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Application
ANDA078216
Marketing category
ANDA
Marketing start
2018-03-21
Marketing end
0000-00-00
Substance
CITALOPRAM HYDROBROMIDE
Active strength
40 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70934-090-30EA - Each70934-0900d85b441-0809-4844-af6e-237605b036ee12018-09-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70934-090CITALOPRAM HYDROBROMIDE TABLET [DENTON PHARMA, INC. DBA NORTHWIND PHARMACEUTICALS]5Legacy NDC20230118_6cd05646-c9f7-03ee-e053-2a91aa0a83cb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70934-090-307093400903030 TABLET in 1 BOTTLE, PLASTIC (70934-090-30) 30 tablet2018-03-210000-00-00NoNoCurrent
70934-090-907093400909090 TABLET in 1 BOTTLE, PLASTIC (70934-090-90) 90 tablet2021-01-200000-00-00NoNoCurrent