Escitalopram
- Product NDC
- 0615-8349
- 11-digit product format
- 006158349
- Labeler code
- 0615
- Product ID
- 0615-8349_173fe9d4-f8a3-4d35-82d4-2f2cf0469949
- 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
- 2013-03-19
- Marketing end
- 2022-04-30
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0615-8349-05 | 00615834905 | 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8349-05) | | 2020-09-04 | 2022-04-30 | No | No | Current |
| 0615-8349-30 | 00615834930 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8349-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK | 6 blister pack | 2020-09-02 | 2022-04-30 | No | No | Current |
| 0615-8349-39 | 00615834939 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8349-39) | | 2020-09-04 | 2022-04-30 | No | No | Current |