Citalopram
- Product NDC
- 50090-3247
- 11-digit product format
- 500903247
- Labeler code
- 50090
- Product ID
- 50090-3247_14d0d816-0fd7-49d7-9bec-a85753046cb9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- citalopram hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA205407
- Marketing category
- ANDA
- Marketing start
- 2015-12-23
- Marketing end
- 0000-00-00
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 20 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