Escitalopram
- Product NDC
- 60760-393
- 11-digit product format
- 607600393
- Labeler code
- 60760
- Product ID
- 60760-393_98d25ae5-7f16-a055-e053-2a95a90a33e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA078032
- Marketing category
- ANDA
- Marketing start
- 2019-11-28
- 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
- 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 |
|---|
| 60760-393-90 | 60760039390 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-393-90) | 2019-11-28 | 0000-00-00 | No | No | Current |