Citalopram
- Product NDC
- 68788-6810
- 11-digit product format
- 687886810
- Labeler code
- 68788
- Product ID
- 68788-6810_ca87bc78-17c8-4b52-867a-ca3f71277acd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA077289
- Marketing category
- ANDA
- Marketing start
- 2016-11-07
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record