Citalopram
- Product NDC
- 70934-539
- 11-digit product format
- 709340539
- Labeler code
- 70934
- Product ID
- 70934-539_ad280f63-c7d8-4444-e053-2a95a90a7e74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Citalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA077045
- Marketing category
- ANDA
- Marketing start
- 2020-02-07
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-539-30 | 70934053930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-539-30) | 2020-02-07 | 0000-00-00 | No | No | Current |
| 70934-539-90 | 70934053990 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-539-90) | 2020-04-03 | 0000-00-00 | No | No | Current |
| 70934-539-97 | 70934053997 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-539-97) | 2020-07-16 | 0000-00-00 | No | No | Current |