Escitalopram
- Product NDC
- 71335-1002
- 11-digit product format
- 713351002
- Labeler code
- 71335
- Product ID
- 71335-1002_aa0ac792-8761-4f81-b6a4-79239182c731
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202389
- Marketing category
- ANDA
- Marketing start
- 2013-03-21
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Escitalopram
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ESCITALOPRAM OXALATE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5U85DBW7LO |
| Rxcui | 351250 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-1002-1 | Escitalopram | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 7 |
| 71335-1002-2 | Escitalopram | 28 in 1 BOTTLE | TABLET, FILM COATED | 28 | | 7 |
| 71335-1002-3 | Escitalopram | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 7 |
| 71335-1002-4 | Escitalopram | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 7 |
| 71335-1002-5 | Escitalopram | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | | 7 |
| 71335-1002-6 | Escitalopram | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 7 |
| 71335-1002-7 | Escitalopram | 45 in 1 BOTTLE | TABLET, FILM COATED | 45 | | 7 |
| 71335-1002-8 | Escitalopram | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1002 | ESCITALOPRAM TABLET, FILM COATED [BRYANT RANCH PREPACK] | 7 | Current NDC, Legacy NDC, 8 package rows | 20250223_d143ec01-9445-42d5-a259-b0b5a7f9445f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1002-1 | 71335100201 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1002-1) | 2018-12-20 | 0000-00-00 | No | No | Current |
| 71335-1002-2 | 71335100202 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1002-2) | 2025-01-29 | 0000-00-00 | No | No | Current |
| 71335-1002-3 | 71335100203 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1002-3) | 2018-11-19 | 0000-00-00 | No | No | Current |
| 71335-1002-4 | 71335100204 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1002-4) | 2018-11-30 | 0000-00-00 | No | No | Current |
| 71335-1002-5 | 71335100205 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-1002-5) | 2025-01-29 | 0000-00-00 | No | No | Current |
| 71335-1002-6 | 71335100206 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1002-6) | 2023-05-10 | 0000-00-00 | No | No | Current |
| 71335-1002-7 | 71335100207 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-1002-7) | 2025-01-29 | 0000-00-00 | No | No | Current |
| 71335-1002-8 | 71335100208 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1002-8) | 2025-01-29 | 0000-00-00 | No | No | Current |