Citalopram
- Product NDC
- 59746-546
- 11-digit product format
- 597460546
- Labeler code
- 59746
- Product ID
- 59746-546_4aa4fe4e-9862-49ef-8370-c0d91a955601
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- citalopram hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Application
- ANDA205407
- Marketing category
- ANDA
- Marketing start
- 2015-12-23
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record