Citalopram
- Product NDC
- 68788-0007
- 11-digit product format
- 687880007
- Labeler code
- 68788
- Product ID
- 68788-0007_f3013718-656d-4a5c-8f22-4900d5777407
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077534
- Marketing category
- ANDA
- Marketing start
- 2014-10-17
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record