Citalopram Hydrobromide
- Product NDC
- 68462-113
- 11-digit product format
- 684620113
- Labeler code
- 68462
- Product ID
- 68462-113_a2e433a6-ad8c-48d9-b52a-398b1168a053
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Glenmark Generics Inc., USA
- Application
- ANDA077654
- Marketing category
- ANDA
- Marketing start
- 2009-02-27
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record