Prescription drug · ANDA

Escitalopram NDC 51655-277

Escitalopram oxalate 10 mg/1 · Tablet, Film coated · Oral · Northwind Health Company, LLC

NDC codes

FDA NDC Directory
Product NDC (as listed)51655-277Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51655-0277Add 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
51655-277-26516550277265165502772690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-26)Marketed from Oct 5, 2022
51655-277-52516550277525165502775230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-277-52)Marketed from Sep 8, 2022

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 — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Northwind Health Company, LLCNDC labeler code 51655
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078032
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 51655-277_48e6f0e2-cba0-fa06-e063-6294a90a296fSPL ID 48e6f0e2-cba0-fa06-e063-6294a90a296fSPL set ID f2b7b0a6-481b-1f6f-e053-2a95a90a2d04RxCUI 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

N451655027726 followed by a unit qualifier and the quantity

Package 51655-0277-26. 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 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 information. 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 )…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51655-277

What is NDC 51655-277?
51655-277 is the product NDC for Escitalopram, Escitalopram oxalate 10 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 2 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?
Northwind Health Company, LLC, NDC labeler code 51655. 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 078032

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

FDA NDC Directory listings under ANDA 078032
ProductStrengthForm · routeLabelerProduct NDC
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralQPharma, Inc.42708-155
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralQPharma, Inc.42708-163
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralSOLCO HEALTHCARE US, LLC43547-280
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralSOLCO HEALTHCARE US, LLC43547-281
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralSOLCO HEALTHCARE US, LLC43547-282
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5312
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6190
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6191
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6534
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6897
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-116
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-284
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-865
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralCoupler LLC67046-0355
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralRedPharm Drug, Inc.67296-1421
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-591
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-592
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-593
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5248
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-7461

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