Citalopram
- Product NDC
- 49999-654
- 11-digit product format
- 499990654
- Labeler code
- 49999
- Product ID
- 49999-654_ad06a464-6f68-4a55-a934-d0ef0d19be1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077289
- Marketing category
- ANDA
- Marketing start
- 2011-11-22
- 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