NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1030Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1030Add 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 NDC11-digit (billing)PackageCopy
71335-1030-1713351030017133510300130 TABLET, FILM COATED in 1 BOTTLE (71335-1030-1)Marketed from Jan 3, 2019
71335-1030-2713351030027133510300228 TABLET, FILM COATED in 1 BOTTLE (71335-1030-2)Marketed from Jan 29, 2025
71335-1030-3713351030037133510300360 TABLET, FILM COATED in 1 BOTTLE (71335-1030-3)Marketed from Feb 6, 2019
71335-1030-4713351030047133510300490 TABLET, FILM COATED in 1 BOTTLE (71335-1030-4)Marketed from Dec 19, 2018
71335-1030-5713351030057133510300510 TABLET, FILM COATED in 1 BOTTLE (71335-1030-5)Marketed from Jan 29, 2025
71335-1030-67133510300671335103006120 TABLET, FILM COATED in 1 BOTTLE (71335-1030-6)Marketed from Jan 29, 2025
71335-1030-771335103007713351030077 TABLET, FILM COATED in 1 BOTTLE (71335-1030-7)Marketed from Jan 29, 2025
71335-1030-87133510300871335103008180 TABLET, FILM COATED in 1 BOTTLE (71335-1030-8)Marketed from Jan 29, 2025
71335-1030-97133510300971335103009100 TABLET, FILM COATED in 1 BOTTLE (71335-1030-9)Marketed from Jun 21, 2022

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 — 10 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 202389
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 71335-1030_c4f98a44-ee66-4051-b968-0ca7711cd0b3SPL ID c4f98a44-ee66-4051-b968-0ca7711cd0b3SPL set ID 4966fd83-ee96-4f87-beb1-dd40d70de445RxCUI 349332UNII 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

N471335103001 followed by a unit qualifier and the quantity

Package 71335-1030-01. 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 oxalate 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 tablet is 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 and LEXAPRO (escitalopram) oral solution. However, due to AbbVie Inc.’s marketing exclusivity rights, this drug product is not labeled with that…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1030

What is NDC 71335-1030?
71335-1030 is the product NDC for Escitalopram, Escitalopram oxalate 10 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 9 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?
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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
escitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-417168788-4171-0168788-4171-0368788-4171-06+2 more
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralCoupler LLC67046-035567046-0355-03
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-456770518-4567-00
escitalopramEscitalopram oxalate 15 mg/1CapsuleOralAlmatica Pharma LLC52427-79552427-0795-30
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-86560687-0865-01
escitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-430070518-4300-0070518-4300-01
escitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralCoupler LLC67046-146567046-1465-03
escitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralCoupler LLC67046-147267046-1472-03
escitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-423970518-4239-0070518-4239-0170518-4239-02+1 more
escitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-872368788-8723-0168788-8723-0368788-8723-06+2 more

All 109 Escitalopram NDCs

Other NDCs under ANDA 202389

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

FDA NDC Directory listings under ANDA 202389
ProductStrengthForm · routeLabelerProduct NDC
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-449
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3069
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-425
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-194
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2058
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-661
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralProficient Rx LP71205-325
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-4915
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralProficient Rx LP71205-344
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-149
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-168
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-169
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralAccord Healthcare Inc.16729-170
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1002
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-236
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-766
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4985

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