escitalopram
- Product NDC
- 68382-102
- 11-digit product format
- 683820102
- Labeler code
- 68382
- Product ID
- 68382-102_1aea2c2e-60fe-4278-8963-58bce4e3fb96
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA077734
- Marketing category
- ANDA
- Marketing start
- 2017-12-07
- Marketing end
- 0000-00-00
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 68382-102-01 | 68382010201 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-102-01) | 2017-12-07 | 0000-00-00 | No | No | Current |
| 68382-102-05 | 68382010205 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-102-05) | 2017-12-07 | 0000-00-00 | No | No | Current |
| 68382-102-06 | 68382010206 | 30 TABLET, FILM COATED in 1 BOTTLE (68382-102-06) | 2017-12-07 | 0000-00-00 | No | No | Current |
| 68382-102-10 | 68382010210 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-102-10) | 2017-12-07 | 0000-00-00 | No | No | Current |
| 68382-102-16 | 68382010216 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-102-16) | 2017-12-07 | 0000-00-00 | No | No | Current |