Citalopram
- Product NDC
- 72162-2517
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077031
- Marketing category
- ANDA
- Substance
- CITALOPRAM HYDROBROMIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2517-1 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2517-1) | 2025-06-09 | | No | Historical |
| 72162-2517-5 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-2517-5) | 2025-06-09 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Citalopram | Bryant Ranch Prepack | 2025-06-11 | HUMAN PRESCRIPTION DRUG LABEL | 100 |