Escitalopram
- Product NDC
- 0615-7953
- 11-digit product format
- 006157953
- Labeler code
- 0615
- Product ID
- 0615-7953_3d9ca837-9178-4ec8-83aa-993cbc2a695a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitslopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA078169
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- Marketing end
- 2022-05-31
- Substance
- ESCITALOPRAM OXALATE
- Active strength
- 5 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 |
|---|
| 0615-7953-39 | 00615795339 | 30 TABLET in 1 BLISTER PACK (0615-7953-39) | 30 tablet | 2016-04-14 | 2022-05-31 | No | No | Current |