Escitalopram
- Product NDC
- 31722-251
- 11-digit product format
- 317220251
- Labeler code
- 31722
- Product ID
- 31722-251_e280a343-4949-4c92-96f7-5744d8cf52c9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals
- Application
- ANDA078604
- Marketing category
- ANDA
- Marketing start
- 2012-09-11
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 04dce598-23c6-b7e7-c3dd-9b9cfd6e1615 | Product name | 6 | 20170718 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 31722-251-90 | EA - Each | 31722-251 | 7a7c9a7e-37f2-4fe7-99df-0af2ddffa1e9 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 349332 | escitalopram oxalate 10 MG Oral Tablet | PSN | 64051fcc-2069-40ad-bf16-f224a435e6f1 | 4 |
| 351250 | escitalopram oxalate 20 MG Oral Tablet | PSN | 64051fcc-2069-40ad-bf16-f224a435e6f1 | 4 |
| 349332 | escitalopram 10 MG Oral Tablet | SCD | 64051fcc-2069-40ad-bf16-f224a435e6f1 | 4 |
| 351250 | escitalopram 20 MG Oral Tablet | SCD | 64051fcc-2069-40ad-bf16-f224a435e6f1 | 4 |
| 349332 | escitalopram (as escitalopram oxalate) 10 MG Oral Tablet | SY | 64051fcc-2069-40ad-bf16-f224a435e6f1 | 4 |
| 351250 | escitalopram (as escitalopram oxalate) 20 MG Oral Tablet | SY | 64051fcc-2069-40ad-bf16-f224a435e6f1 | 4 |