Escitalopram
- Product NDC
- 70518-2430
- 11-digit product format
- 705182430
- Labeler code
- 70518
- Product ID
- 70518-2430_c93604db-aa5a-8da7-e053-2a95a90a2623
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078032
- Marketing category
- ANDA
- Marketing start
- 2019-11-18
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 70518-2430 | ESCITALOPRAM TABLET, FILM COATED [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250316_3fdf5482-9945-4014-82d5-054209fe46de.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2430-0 | 70518243000 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2430-0) | 2019-11-18 | 0000-00-00 | No | No | Current |