Prescription drug · ANDA
Escitalopram (escitalopram oxalate) NDC 71205-193
Escitalopram oxalate 20 mg/1 · Tablet, Film coated · Oral · Proficient Rx LP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71205-193-30 | 71205019330 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-193-30)Marketed from Jan 1, 2019 | |
| 71205-193-60 | 71205019360 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-193-60)Marketed from Jan 1, 2019 | |
| 71205-193-90 | 71205019390 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-193-90)Marketed from Jan 1, 2019 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Escitalopram
- Generic name (nonproprietary)
- escitalopram oxalate
- Active ingredients
- Escitalopram oxalate — 20 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Proficient Rx LP
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090432
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 71205-193_e3bdc297-e10a-4632-bf0b-5214ffb84e38SPL ID e3bdc297-e10a-4632-bf0b-5214ffb84e38SPL set ID 52df055d-b1c8-4de2-8545-ef08b5bf9c39RxCUI 351250UNII 5U85DBW7LOUPC 0371205193300
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N471205019330followed by a unit qualifier and the quantityPackage 71205-0193-30. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
Escitalopram oxalate is a selective serotonin reuptake inhibitor (SSRI) indicated for: • Acute and Maintenance Treatment of Major Depressive Disorder (MDD) in adults and adolescents aged 12 to 17 years (1.1) • Acute Treatment of Generalized Anxiety Disorder (GAD) in adults (1.2) 1.1 Major Depressive Disorder Escitalopram tablets are indicated for the acute and maintenance treatment of major depressive disorder in adults and in adolescents 12 to 17 years of age [see Clinical Studies (14.1) ] . A major depressive episode (DSM-IV) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed or dysphoric mood that usually interferes with daily functioning, and …
Excerpt only. Read the full label for complete information.
Other NDCs under ANDA 090432
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Escitalopramescitalopram oxalate | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-311 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6023 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8475 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8476 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | Asclemed USA, Inc. | 76420-721 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Asclemed USA, Inc. | 76420-722 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Asclemed USA, Inc. | 76420-723 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-147 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-374 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | American Health Packaging | 68084-617 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8477 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-373 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | American Health Packaging | 68084-618 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-375 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6496 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-168 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-9687 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Advanced Rx Pharmacy of Tennessee, LLC | 80425-0375 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | QPharma, Inc. | 42708-077 |
| Escitalopramescitalopram oxalate | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-590 |
- openFDA data updated
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