escitalopram
- Product NDC
- 70771-1147
- 11-digit product format
- 707711147
- Labeler code
- 70771
- Product ID
- 70771-1147_9516c1f3-9d94-46aa-9516-35f68c184ad8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA077734
- Marketing category
- ANDA
- Marketing start
- 2017-12-07
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70771-1147 | ESCITALOPRAM TABLET, FILM COATED [ZYDUS LIFESCIENCES LIMITED] | 4 | Legacy NDC | 20221109_76d0e2a8-2ed2-4596-9179-8c360f4a0978.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70771-1147-0 | 70771114700 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1147-0) | 2017-12-07 | 0000-00-00 | No | No | Current |
| 70771-1147-1 | 70771114701 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1147-1) | 2017-12-07 | 0000-00-00 | No | No | Current |
| 70771-1147-3 | 70771114703 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1147-3) | 2017-12-07 | 0000-00-00 | No | No | Current |
| 70771-1147-5 | 70771114705 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1147-5) | 2017-12-07 | 0000-00-00 | No | No | Current |
| 70771-1147-9 | 70771114709 | 90 TABLET, FILM COATED in 1 BOTTLE (70771-1147-9) | 2017-12-07 | 0000-00-00 | No | No | Current |