Citalopram Hydrobromide
- Product NDC
- 68645-559
- 11-digit product format
- 686450559
- Labeler code
- 68645
- Product ID
- 68645-559_e90d8ec9-8436-bd24-e053-2995a90a8e4c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2007-10-18
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68645-559 | CITALOPRAM HYDROBROMIDE TABLET [LEGACY PHARMACEUTICAL PACKAGING, LLC] | 10 | Legacy NDC | 20250124_719276c0-ec1f-4bb4-9cea-e104202689c9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68645-559-54 | 68645055954 | 30 TABLET in 1 BOTTLE (68645-559-54) | 30 tablet | 2007-10-18 | 0000-00-00 | No | No | Current |