NDC 70934-304

Citalopram

Citalopram Hydrobromide

Citalopram is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. The primary component is Citalopram Hydrobromide.

Product ID70934-304_8a815202-37ec-194f-e053-2a95a90a22d4
NDC70934-304
Product TypeHuman Prescription Drug
Proprietary NameCitalopram
Generic NameCitalopram Hydrobromide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2019-03-05
Marketing CategoryANDA / ANDA
Application NumberANDA077031
Labeler NameDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameCITALOPRAM HYDROBROMIDE
Active Ingredient Strength20 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70934-304-30

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-304-30)
Marketing Start Date2019-03-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70934-304-60 [70934030460]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-01-13

NDC 70934-304-90 [70934030490]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-30

NDC 70934-304-30 [70934030430]

Citalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA077031
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-03-05

Drug Details

Active Ingredients

IngredientStrength
CITALOPRAM HYDROBROMIDE20 mg/1

Pharmacological Class

  • Serotonin Reuptake Inhibitor [EPC]
  • Serotonin Uptake Inhibitors [MoA]

NDC Crossover Matching brand name "Citalopram" or generic name "Citalopram Hydrobromide"

NDCBrand NameGeneric Name
0054-0062CitalopramCitalopram
0121-0848CitalopramCitalopram Hydrobromide
0121-1696CitalopramCitalopram Hydrobromide
0185-0371CitalopramCitalopram Hydrobromide
0185-0372CitalopramCitalopram Hydrobromide
0185-0373CitalopramCitalopram Hydrobromide
0378-6231Citalopramcitalopram
0378-6232Citalopramcitalopram
0378-6233Citalopramcitalopram
0615-6510CitalopramCitalopram
0615-6511CitalopramCitalopram
0615-6512CitalopramCitalopram
0615-8022CitalopramCitalopram Hydrobromide
0615-8023CitalopramCitalopram Hydrobromide
0615-8141CitalopramCitalopram Hydrobromide
0713-4740CitalopramCitalopram Tablets
68071-1970CitalopramCitalopram
68071-3042CitalopramCitalopram
68071-3034CitalopramCitalopram
68071-3357CitalopramCitalopram
68071-4291CitalopramCitalopram
68071-4604CitalopramCitalopram
68071-4477CitalopramCitalopram
68071-4324CitalopramCitalopram
68084-737CitalopramCitalopram
68084-744CitalopramCitalopram
68788-6810CitalopramCitalopram
68788-0005CitalopramCitalopram
68788-0007CitalopramCitalopram
69097-822CitalopramCitalopram
69097-824CitalopramCitalopram
69097-823CitalopramCitalopram
70518-0449CitalopramCitalopram
70518-0561CitalopramCitalopram
71335-0541CitalopramCitalopram
71335-0573CitalopramCitalopram
71335-0712CitalopramCitalopram
71335-0656CitalopramCitalopram
0713-4741CitalopramCitalopram
0713-4742CitalopramCitalopram
10544-149CitalopramCitalopram
10544-179CitalopramCitalopram
10544-006CitalopramCitalopram
10544-150CitalopramCitalopram
10544-182CitalopramCitalopram
13107-005CitalopramCitalopram
13107-007CitalopramCitalopram
13107-006CitalopramCitalopram
21695-031CitalopramCitalopram
21695-032CitalopramCitalopram

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.