Citalopram
- Product NDC
- 63629-6691
- 11-digit product format
- 636296691
- Labeler code
- 63629
- Product ID
- 63629-6691_8a814f52-348f-44da-abea-f2ed95708c57
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- citalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077042
- Marketing category
- ANDA
- Marketing start
- 2008-07-28
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 63629-6691-1 | 63629669101 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-6691-1) | 2015-08-25 | 0000-00-00 | No | No | Current |
| 63629-6691-2 | 63629669102 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-6691-2) | 2015-08-25 | 0000-00-00 | No | No | Current |