What is NDC 71335-2960?

71335-2960 is the product NDC for escitalopram, Escitalopram oxalate 20 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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 71335-2960 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2960Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2960Add 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
71335-2960-1	7133529600171335296001	1000 TABLET, FILM COATED in 1 BOTTLE (71335-2960-1)Marketed from Oct 22, 2025

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: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090939
Marketing start: Sep 11, 2012
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 71335-2960_2239931d-ee90-40e9-a5bb-b5c7f0aa9be0SPL ID 2239931d-ee90-40e9-a5bb-b5c7f0aa9be0SPL set ID 1d2f83c1-8ffe-48f3-a084-150289001743RxCUI 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

N471335296001 followed by a unit qualifier and the quantity

Package 71335-2960-01. 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 Jun 12, 2026. 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.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2960

What is NDC 71335-2960?: 71335-2960 is the product NDC for escitalopram, Escitalopram oxalate 20 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. 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?: Bryant Ranch Prepack, NDC labeler code 71335. 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 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

All 109 escitalopram NDCs

Other NDCs under ANDA 090939

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 090939
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 20 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4171
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	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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