Citalopram
- Product NDC
- 50090-7039
- 11-digit product format
- 500907039
- Labeler code
- 50090
- Product ID
- 50090-7039_c28df410-62de-435b-b371-46b9130a831e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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 |
|---|
| 50090-7039-0 | 50090703900 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7039-0) | 2024-01-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Citalopram | A-S Medication Solutions | 2024-08-21 | Human Prescription Drug Label | 12 |