Escitalopram
- Product NDC
- 71335-0658
- 11-digit product format
- 713350658
- Labeler code
- 71335
- Product ID
- 71335-0658_69d581c1-9ee5-4d9b-8ee8-fa9d310e8553
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram Oxalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090432
- Marketing category
- ANDA
- Marketing start
- 2012-09-11
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 20 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0658-1 | 71335065801 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0658-1) | 2018-08-02 | 0000-00-00 | No | No | Current |
| 71335-0658-2 | 71335065802 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0658-2) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0658-3 | 71335065803 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0658-3) | 2018-07-24 | 0000-00-00 | No | No | Current |
| 71335-0658-4 | 71335065804 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0658-4) | 2018-08-24 | 0000-00-00 | No | No | Current |
| 71335-0658-5 | 71335065805 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0658-5) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0658-6 | 71335065806 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0658-6) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0658-7 | 71335065807 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-0658-7) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0658-8 | 71335065808 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0658-8) | 2021-12-27 | 0000-00-00 | No | No | Current |