Citalopram
- Product NDC
- 50090-2732
- 11-digit product format
- 500902732
- Labeler code
- 50090
- Product ID
- 50090-2732_1ec657d2-7f29-478c-8d15-6e9571ce9dff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077289
- Marketing category
- ANDA
- Marketing start
- 2010-04-06
- 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