Citalopram Hydrobromide
- Product NDC
- 54838-540
- 11-digit product format
- 548380540
- Labeler code
- 54838
- Product ID
- 54838-540_8e2a2cfe-8458-4e42-b0a2-aefd6993b0a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA077629
- Marketing category
- ANDA
- Marketing start
- 2006-06-14
- Marketing end
- 2023-10-31
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 10 mg/5mL
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 54838-540-70 | 54838054070 | 240 mL in 1 BOTTLE, PLASTIC (54838-540-70) | 240 ml | 2006-06-14 | 0000-00-00 | No | No | Current |