Citalopram
- Product NDC
- 71610-413
- 11-digit product format
- 716100413
- Labeler code
- 71610
- Product ID
- 71610-413_fc10ffe3-e320-4a92-9b34-1f56d369691b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA077031
- Marketing category
- ANDA
- Marketing start
- 2004-10-28
- 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
- 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 |
|---|
| 71610-413-60 | 71610041360 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-413-60) | 2020-04-03 | No | No | Historical |