Citalopram
- Product NDC
- 0713-4742
- 11-digit product format
- 007134742
- Labeler code
- 0713
- Product ID
- 0713-4742_8eadc3e4-81a3-4b3b-aa1c-1dc65151f94c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram Tablet
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cosette Pharmaceuticals, Inc.
- Application
- ANDA077048
- Marketing category
- ANDA
- Marketing start
- 2015-12-02
- 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
- 2021-12-31
- 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 |
|---|
| 0713-4742-01 | 00713474201 | 100 TABLET in 1 BOTTLE (0713-4742-01) | 100 tablet | 2015-12-02 | 0000-00-00 | No | No | Current |
| 0713-4742-05 | 00713474205 | 500 TABLET in 1 BOTTLE (0713-4742-05) | 500 tablet | 2015-12-02 | 0000-00-00 | No | No | Current |