Citalopram
- Product NDC
- 63629-6761
- 11-digit product format
- 636296761
- Labeler code
- 63629
- Product ID
- 63629-6761_26647185-e6c1-4675-b35b-920c6788c037
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077534
- Marketing category
- ANDA
- Marketing start
- 2011-01-01
- 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
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6761-1 | 63629676101 | 90 TABLET in 1 BOTTLE (63629-6761-1) | 90 tablet | 2015-09-28 | 0000-00-00 | No | No | Current |
| 63629-6761-2 | 63629676102 | 30 TABLET in 1 BOTTLE (63629-6761-2) | 30 tablet | 2015-09-28 | 0000-00-00 | No | No | Current |