Citalopram Hydrobromide
- Product NDC
- 68071-1830
- 11-digit product format
- 680711830
- Labeler code
- 68071
- Product ID
- 68071-1830_2a9687f5-a055-ea3f-e063-6294a90a9db3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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 |
|---|
| 68071-1830-1 | 68071183001 | 100 TABLET in 1 BOTTLE (68071-1830-1) | 100 tablet | 2021-06-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Citalopram Tablets, USP | NuCare Pharmaceuticals,Inc. | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL | 2 |