Prescription drug · ANDA
escitalopram NDC 68788-4171
Escitalopram oxalate 20 mg/1 · Tablet, Film coated · Oral · Preferred Pharmaceuticals Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 68788-4171-1 | 6878841710168788417101 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-4171-1)Marketed from Jul 24, 2026 | |
| 68788-4171-3 | 6878841710368788417103 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-4171-3)Marketed from Jul 24, 2026 | |
| 68788-4171-6 | 6878841710668788417106 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-4171-6)Marketed from Jul 24, 2026 | |
| 68788-4171-8 | 6878841710868788417108 | 28 TABLET, FILM COATED in 1 BOTTLE (68788-4171-8)Marketed from Jul 24, 2026 | |
| 68788-4171-9 | 6878841710968788417109 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-4171-9)Marketed from Jul 24, 2026 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
- Active ingredients
- Escitalopram oxalate — 20 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Preferred Pharmaceuticals Inc.NDC labeler code 68788
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090939
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 68788-4171_9ddd1f24-3ebd-4307-bb23-6acd742cd140SPL ID 9ddd1f24-3ebd-4307-bb23-6acd742cd140SPL set ID 9ddd1f24-3ebd-4307-bb23-6acd742cd140RxCUI 351250UNII 5U85DBW7LO
- 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
N468788417101followed by a unit qualifier and the quantityPackage 68788-4171-01. 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 is a selective serotonin reuptake inhibitor (SSRI) indicated for the: • treatment of major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older ( 1 ) • treatment of generalized anxiety disorder (GAD) in adults ( 1 ) Escitalopram tablets are indicated for the treatment of: • major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older. • generalized anxiety disorder (GAD) in adults. Additional pediatric use information is approved for AbbVie Inc.’s LEXAPRO ® (escitalopram) tablets. However, due to AbbVie Inc.’s marketing exclusivity rights, this drug product is not labeled with that information.
Excerpt only. Read the full label for complete information.
About NDC 68788-4171
- What is NDC 68788-4171?
- 68788-4171 is the product NDC for escitalopram, Escitalopram oxalate 20 mg/1 tablet, film coated, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- escitalopram.
- What is the active ingredient?
- Escitalopram oxalate.
- Who is the labeler?
- Preferred Pharmaceuticals Inc., NDC labeler code 68788. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for escitalopram?
- 108 other product NDCs are listed under this name. See all escitalopram NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other escitalopram products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-0355 | 67046-0355-03 |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4567 | 70518-4567-00 |
| escitalopram | Escitalopram oxalate 15 mg/1 | CapsuleOral | Almatica Pharma LLC | 52427-795 | 52427-0795-30 |
| Escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | American Health Packaging | 60687-865 | 60687-0865-01 |
| escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4300 | 70518-4300-0070518-4300-01 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1465 | 67046-1465-03 |
| escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1472 | 67046-1472-03 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4239 | 70518-4239-0070518-4239-0170518-4239-02+1 more |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8723 | 68788-8723-0168788-8723-0368788-8723-06+2 more |
| escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-895 | 60760-0895-3060760-0895-90 |
Other NDCs under ANDA 090939
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 |
|---|---|---|---|---|
| escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Major Pharmaceuticals | 0904-6426 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Major Pharmaceuticals | 0904-6427 |
| escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | Torrent Pharmaceuticals Limited | 13668-135 |
| escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Torrent Pharmaceuticals Limited | 13668-136 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Torrent Pharmaceuticals Limited | 13668-137 |
| escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Cardinal Health 107, LLC | 55154-6893 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Cardinal Health 107, LLC | 55154-7288 |
| escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-2903 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-2960 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2240 |
| escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2241 |
| escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 72162-2242 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | TabletOral | Direct_Rx | 72189-438 |
| escitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-761 |
| escitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8371 |
| escitalopram oxalate | Escitalopram oxalate 5 mg/1 | TabletOral | Proficient Rx LP | 71205-313 |
| escitalopram oxalate | Escitalopram oxalate 10 mg/1 | TabletOral | Proficient Rx LP | 71205-792 |
| escitalopram oxalate | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-0322 |
| escitalopram oxalate | Escitalopram oxalate 20 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-0685 |
| escitalopram oxalate | Escitalopram oxalate 5 mg/1 | TabletOral | Quallent Pharmaceuticals Health LLC | 82009-035 |
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