Citalopram
- Product NDC
- 68084-744
- 11-digit product format
- 680840744
- Labeler code
- 68084
- Product ID
- 68084-744_de592900-2fd5-7409-e053-2995a90abb13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Hydrobromide
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077031
- Marketing category
- ANDA
- Marketing start
- 2014-03-17
- Marketing end
- 2023-07-31
- Substance
- CITALOPRAM HYDROBROMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68084-744-01 | 68084074401 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-744-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-744-11) | 100 blister pack | 2014-03-17 | 0000-00-00 | No | No | Current |