Escitalopram
- Product NDC
- 0615-8366
- 11-digit product format
- 006158366
- Labeler code
- 0615
- Product ID
- 0615-8366_b94038e3-753b-4d35-9213-2a39ab567f9d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- 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
- 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 |
|---|
| 0615-8366-05 | 00615836605 | 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8366-05) | 2020-12-02 | 0000-00-00 | No | No | Current |
| 0615-8366-39 | 00615836639 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8366-39) | 2020-12-02 | 0000-00-00 | No | No | Current |