Citalopram Hydrobromide
- Product NDC
- 50090-2888
- 11-digit product format
- 500902888
- Labeler code
- 50090
- Product ID
- 50090-2888_e64d836f-e882-4ccb-a0f0-c6c3964e004e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2007-10-18
- 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
FDA-Initiated Inactive NDC Indexing#