Escitalopram
- Product NDC
- 50090-5830
- 11-digit product format
- 500905830
- Labeler code
- 50090
- Product ID
- 50090-5830_e5d3ba78-1f7b-4561-8a56-048dd2e3ab66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitslopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078169
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5830 | ESCITALOPRAM (ESCITSLOPRAM) TABLET [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC | 20230317_c1945926-4638-4e42-b51c-1c152ab5c8eb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5830-0 | 50090583000 | 30 TABLET in 1 BOTTLE (50090-5830-0) | 30 tablet | 2021-10-26 | 0000-00-00 | No | No | Current |
| 50090-5830-1 | 50090583001 | 90 TABLET in 1 BOTTLE (50090-5830-1) | 90 tablet | 2021-10-26 | 0000-00-00 | No | No | Current |