escitalopram oxalate
- Product NDC
- 70518-1697
- 11-digit product format
- 705181697
- Labeler code
- 70518
- Product ID
- 70518-1697_962c545a-2812-4a05-e053-2a95a90a1418
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram oxalate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090939
- Marketing category
- ANDA
- Marketing start
- 2018-11-28
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1697 | ESCITALOPRAM OXALATE TABLET [REMEDYREPACK INC.] | 7 | Legacy NDC | 20241129_99c13917-c35f-4a4f-b1aa-0e2f8c166ab0.zip |