Citalopram
- Product NDC
- 68071-4604
- 11-digit product format
- 680714604
- Labeler code
- 68071
- Product ID
- 68071-4604_c084663e-5f9b-189d-e053-2995a90addaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077031
- Marketing category
- ANDA
- Marketing start
- 2004-10-28
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4604-3 | 68071460403 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4604-3) | 2018-10-17 | 0000-00-00 | No | No | Current |
| 68071-4604-5 | 68071460405 | 15 TABLET, FILM COATED in 1 BOTTLE (68071-4604-5) | 2018-10-17 | 0000-00-00 | No | No | Current |
| 68071-4604-6 | 68071460406 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4604-6) | 2018-10-17 | 0000-00-00 | No | No | Current |
| 68071-4604-9 | 68071460409 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-4604-9) | 2018-10-17 | 0000-00-00 | No | No | Current |