Citalopram Hydrobromide
- Product NDC
- 71205-764
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078216
- Marketing category
- ANDA
- Substance
- CITALOPRAM HYDROBROMIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-764-30 | 30 TABLET in 1 BOTTLE (71205-764-30) | 2023-02-14 | | No | Historical |
| 71205-764-60 | 60 TABLET in 1 BOTTLE (71205-764-60) | 2023-02-14 | | No | Historical |
| 71205-764-90 | 90 TABLET in 1 BOTTLE (71205-764-90) | 2023-02-14 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Citalopram Hydrobromide | Proficient Rx LP | 2023-02-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |