Citalopram Hydrobromide
- Product NDC
- 50090-6846
- 11-digit product format
- 500906846
- Labeler code
- 50090
- Product ID
- 50090-6846_3e57b69e-a9bd-4480-9466-aabbc6208e32
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2007-10-18
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 20 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6846-0 | 50090684600 | 90 TABLET in 1 BOTTLE (50090-6846-0) | 90 tablet | 2023-11-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Citalopram Hydrobromide | A-S Medication Solutions | 2023-12-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |