Citalopram
- Product NDC
- 0121-0848
- 11-digit product format
- 001210848
- Labeler code
- 0121
- Product ID
- 0121-0848_860688c2-1d25-4f79-e053-2991aa0a8c68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Pharmaceutical Associates, Inc.
- Application
- ANDA077629
- Marketing category
- ANDA
- Marketing start
- 2006-06-14
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0121-0848-40 | 00121084840 | 4 TRAY in 1 CASE (0121-0848-40) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (0121-0848-05) | 4 tray | 2019-04-08 | 0000-00-00 | No | No | Current |