Escitalopram
- Product NDC
- 63629-4688
- 11-digit product format
- 636294688
- Labeler code
- 63629
- Product ID
- 63629-4688_2f8d7728-b2e0-4061-8118-9c58004a2bc4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076765
- Marketing category
- ANDA
- Marketing start
- 2012-03-14
- 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
- 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 |
|---|
| 63629-4688-1 | 63629468801 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4688-1) | 2012-03-29 | 0000-00-00 | No | No | Current |
| 63629-4688-2 | 63629468802 | 28 TABLET, FILM COATED in 1 BOTTLE (63629-4688-2) | 2012-03-29 | 0000-00-00 | No | No | Current |
| 63629-4688-3 | 63629468803 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4688-3) | 2012-03-29 | 0000-00-00 | No | No | Current |
| 63629-4688-4 | 63629468804 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4688-4) | 2012-03-29 | 0000-00-00 | No | No | Current |
| 63629-4688-5 | 63629468805 | 10 TABLET, FILM COATED in 1 BOTTLE (63629-4688-5) | 2012-03-29 | 0000-00-00 | No | No | Current |
| 63629-4688-6 | 63629468806 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-4688-6) | 2012-03-29 | 0000-00-00 | No | No | Current |
| 63629-4688-7 | 63629468807 | 7 TABLET, FILM COATED in 1 BOTTLE (63629-4688-7) | 2012-03-29 | 0000-00-00 | No | No | Current |