Escitalopram Oxalate
- Product NDC
- 70518-3151
- 11-digit product format
- 705183151
- Labeler code
- 70518
- Product ID
- 70518-3151_e6d91c95-5eb5-f9fb-e053-2995a90a54d5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078604
- Marketing category
- ANDA
- Marketing start
- 2021-07-14
- 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
- 2023-12-31
- 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 |
|---|
| 70518-3151-0 | 70518315100 | 30 POUCH in 1 BOX (70518-3151-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-3151-1) | 30 pouch | 2021-07-14 | 0000-00-00 | No | No | Current |