Citalopram
- Product NDC
- 68788-7899
- 11-digit product format
- 687887899
- Labeler code
- 68788
- Product ID
- 68788-7899_ff029fae-f691-4467-b274-c8cd558058d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA077534
- Marketing category
- ANDA
- Marketing start
- 2021-05-14
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7899-3 | 68788789903 | 30 TABLET in 1 BOTTLE (68788-7899-3) | 30 tablet | 2021-05-14 | 0000-00-00 | No | No | Current |
| 68788-7899-6 | 68788789906 | 60 TABLET in 1 BOTTLE (68788-7899-6) | 60 tablet | 2021-05-14 | 0000-00-00 | No | No | Current |
| 68788-7899-9 | 68788789909 | 90 TABLET in 1 BOTTLE (68788-7899-9) | 90 tablet | 2021-05-14 | 0000-00-00 | No | No | Current |