escitalopram oxalate
- Product NDC
- 60760-157
- 11-digit product format
- 607600157
- Labeler code
- 60760
- Product ID
- 60760-157_7a8e2c72-4c43-2680-e053-2991aa0a73d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram oxalate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA090939
- Marketing category
- ANDA
- Marketing start
- 2017-12-15
- 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
- 2020-12-31
- 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 |
|---|
| 60760-157-30 | 60760015730 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-157-30) | 30 tablet | 2017-12-15 | 0000-00-00 | No | No | Current |
| 60760-157-90 | 60760015790 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-157-90) | 90 tablet | 2018-06-18 | 0000-00-00 | No | No | Current |