Escitalopram
- Product NDC
- 70934-650
- 11-digit product format
- 709340650
- Labeler code
- 70934
- Product ID
- 70934-650_aa8f5abd-a93b-e3ce-e053-2a95a90a5c39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA078032
- Marketing category
- ANDA
- Marketing start
- 2020-04-02
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-650-90 | 70934065090 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-650-90) | 2020-04-02 | 0000-00-00 | No | No | Current |