Escitalopram
- Product NDC
- 0093-5852
- 11-digit product format
- 000935852
- Labeler code
- 0093
- Product ID
- 0093-5852_c4634b47-1b92-4acf-bbb2-01241d18989b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Escitalopram
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA076765
- Marketing category
- ANDA
- Marketing start
- 2012-03-14
- Marketing end
- 2021-11-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| ESCITALOPRAM OXALATE | ACTIVE INGREDIENT | 5U85DBW7LO | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| ESCITALOPRAM OXALATE | ACTIVE INGREDIENT | 5U85DBW7LO | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| ESCITALOPRAM OXALATE | ACTIVE INGREDIENT | 5U85DBW7LO | ESCITALOPRAM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS] | 1 | |
| ESCITALOPRAM | ACTIVE MOIETY | 4O4S742ANY | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| ESCITALOPRAM | ACTIVE MOIETY | 4O4S742ANY | ESCITALOPRAM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS] | 1 | |
| ESCITALOPRAM | ACTIVE MOIETY | 4O4S742ANY | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | ESCITALOPRAM TABLET, FILM COATED [STAT RX USA LLC] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | ESCITALOPRAM TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | |
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 |
|---|
| 0093-5852-01 | 00093585201 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5852-01) | 2012-03-14 | 2021-11-30 | No | No | Current |
| 0093-5852-05 | 00093585205 | 500 TABLET, FILM COATED in 1 BOTTLE (0093-5852-05) | 2012-05-03 | 2021-11-30 | No | No | Current |