Citalopram Hydrobromide
- Product NDC
- 80425-0309
- 11-digit product format
- 804250309
- Labeler code
- 80425
- Product ID
- 80425-0309_2a9bf621-afbd-7627-e063-6294a90a77a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- ANDA077031
- Marketing category
- ANDA
- Marketing start
- 2023-04-06
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| I1E9D14F36 | CITALOPRAM HYDROBROMIDE | 59729-32-7 | CITALOPRAM HYDROBROMIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 80425-0309-1 | 80425030901 | 30 TABLET, FILM COATED in 1 BOTTLE (80425-0309-1) | 2023-04-06 | No | No | Historical |
| 80425-0309-2 | 80425030902 | 60 TABLET, FILM COATED in 1 BOTTLE (80425-0309-2) | 2023-04-06 | No | No | Historical |
| 80425-0309-3 | 80425030903 | 90 TABLET, FILM COATED in 1 BOTTLE (80425-0309-3) | 2023-04-06 | No | No | Historical |