Escitalopram
- Product NDC
- 60760-170
- 11-digit product format
- 607600170
- Labeler code
- 60760
- Product ID
- 60760-170_f06e4d37-5f30-d60c-e053-2995a90a4634
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA202389
- Marketing category
- ANDA
- Marketing start
- 2013-03-21
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-170-30 | 60760017030 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-170-30) | 2017-11-21 | 0000-00-00 | No | No | Current |
| 60760-170-90 | 60760017090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-170-90) | 2017-11-21 | 0000-00-00 | No | No | Current |