Citalopram Hydrobromide
- Product NDC
- 0904-6086
- 11-digit product format
- 009046086
- Labeler code
- 0904
- Product ID
- 0904-6086_e81f54a5-116f-4c8d-9c29-76fa7b2f22f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA078216
- Marketing category
- ANDA
- Marketing start
- 2009-11-02
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6086-61 | 00904608661 | 100 BLISTER PACK in 1 CARTON (0904-6086-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2009-11-02 | 0000-00-00 | No | No | Current |