What is NDC 52427-795?

52427-795 is the product NDC for escitalopram, Escitalopram oxalate 15 mg/1 capsule, listed with the FDA by Almatica Pharma LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Almatica Pharma LLC, NDC labeler code 52427. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

escitalopram NDC 52427-795 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)52427-795Labeler and product segments. Claims need a package NDC.

Product NDC at billing width52427-0795Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
52427-795-30	5242707953052427079530	30 CAPSULE in 1 BOTTLE (52427-795-30)Marketed from Oct 6, 2025

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
Active ingredients: Escitalopram oxalate — 15 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Almatica Pharma LLCNDC labeler code 52427
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 219130
Marketing start: Oct 6, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 52427-795_4caf6d36-950a-522b-5914-079783778c6fSPL ID 4caf6d36-950a-522b-5914-079783778c6fSPL set ID c0401570-a3b0-bef2-7365-c23dc952b8b6RxCUI 2725159UNII 5U85DBW7LOUPC 0352427795305
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

N452427079530 followed by a unit qualifier and the quantity

Package 52427-0795-30. 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 Aug 31, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Escitalopram Capsules are indicated for the treatment of: Major depressive disorder (MDD) in adults younger than 65 years of age [see Dosage and Administration ( 2.1 )] and pediatric patients 12 years of age and older. Generalized anxiety disorder (GAD) in adults younger than 65 years of age [see Dosage and Administration (2.1)] . Additional pediatric use information is approved for AbbVie Inc.’s LEXAPRO (escitalopram) tablets and LEXAPRO (escitalopram) oral solution. However, due to AbbVie Inc.’s marketing exclusivity rights, this drug product is not labeled with that information. Escitalopram Capsules are a selective serotonin reuptake inhibitor (SSRI) indicated for the treatment of: ( 1 )…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 52427-795

What is NDC 52427-795?: 52427-795 is the product NDC for escitalopram, Escitalopram oxalate 15 mg/1 capsule, listed with the FDA by Almatica Pharma LLC. It has 1 package NDC, 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?: Almatica Pharma LLC, NDC labeler code 52427. 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.

Other finished products listed under the same name: strengths, forms and labelers.

Other escitalopram NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
escitalopram	Escitalopram oxalate 20 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4171	68788-4171-0168788-4171-0368788-4171-06+2 more
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 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

All 109 escitalopram NDCs