Citalopram Hydrobromide
- Product NDC
- 55111-342
- 11-digit product format
- 551110342
- Labeler code
- 55111
- Product ID
- 55111-342_77a66875-7c9c-8c98-9ddf-99f2bfaac6ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Dr. Reddy's Laboratories Limited
- Application
- ANDA077038
- Marketing category
- ANDA
- Marketing start
- 2004-10-28
- 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
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 55111-342-01 | 55111034201 | 100 TABLET, FILM COATED in 1 BOTTLE (55111-342-01) | | 2004-10-28 | 0000-00-00 | No | No | Current |
| 55111-342-05 | 55111034205 | 500 TABLET, FILM COATED in 1 BOTTLE (55111-342-05) | | 2004-10-28 | 0000-00-00 | No | No | Current |
| 55111-342-30 | 55111034230 | 30 TABLET, FILM COATED in 1 BOTTLE (55111-342-30) | | 2004-10-28 | 0000-00-00 | No | No | Current |
| 55111-342-60 | 55111034260 | 60 TABLET, FILM COATED in 1 BOTTLE (55111-342-60) | | 2004-10-28 | 0000-00-00 | No | No | Current |
| 55111-342-78 | 55111034278 | 10 BLISTER PACK in 1 CARTON (55111-342-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-342-79) | 10 blister pack | 2004-10-28 | 0000-00-00 | No | No | Current |