NDC codes

FDA NDC Directory
Product NDC (as listed)68084-618Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68084-0618Add 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
68084-618-016808406180168084061801100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-618-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-618-11)Marketed from Oct 8, 2012

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 oxalate
Active ingredients
Escitalopram oxalate — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
American Health PackagingNDC labeler code 68084
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090432
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 68084-618_30deba4d-85ab-64e3-e063-6394a90a085eSPL ID 30deba4d-85ab-64e3-e063-6394a90a085eSPL set ID 3019a647-9bcf-48cf-928c-0467f9b921a8RxCUI 349332, 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

N468084061801 followed by a unit qualifier and the quantity

Package 68084-0618-01. 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 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. 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)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68084-618

What is NDC 68084-618?
68084-618 is the product NDC for Escitalopram (escitalopram oxalate), Escitalopram oxalate 20 mg/1 tablet, film coated, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Escitalopram (Escitalopram Oxalate).
What is the active ingredient?
Escitalopram oxalate.
Who is the labeler?
American Health Packaging, NDC labeler code 68084. 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 090432

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

FDA NDC Directory listings under ANDA 090432
ProductStrengthForm · routeLabelerProduct NDC
Escitalopramescitalopram oxalateEscitalopram oxalate 5 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8475
Escitalopramescitalopram oxalateEscitalopram oxalate 10 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8476
Escitalopramescitalopram oxalateEscitalopram oxalate 20 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8477
Escitalopramescitalopram oxalateEscitalopram oxalate 10 mg/1Tablet, Film coatedOralQPharma, Inc.42708-077
Escitalopramescitalopram oxalateEscitalopram oxalate 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6023
Escitalopramescitalopram oxalateEscitalopram oxalate 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-6496
Escitalopramescitalopram oxalateEscitalopram oxalate 20 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-147
Escitalopramescitalopram oxalateEscitalopram oxalate 20 mg/1Tablet, Film coatedOralSt. Mary's Medical Park Pharmacy60760-590
Escitalopramescitalopram oxalateEscitalopram oxalate 5 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-373
Escitalopramescitalopram oxalateEscitalopram oxalate 10 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-374
Escitalopramescitalopram oxalateEscitalopram oxalate 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-375
Escitalopramescitalopram oxalateEscitalopram oxalate 10 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-617
Escitalopramescitalopram oxalateEscitalopram oxalate 10 mg/1Tablet, Film coatedOralProficient Rx LP71205-168
Escitalopramescitalopram oxalateEscitalopram oxalate 20 mg/1Tablet, Film coatedOralProficient Rx LP71205-193
Escitalopramescitalopram oxalateEscitalopram oxalate 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-9687
Escitalopramescitalopram oxalateEscitalopram oxalate 20 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-311
Escitalopramescitalopram oxalateEscitalopram oxalate 5 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-721
Escitalopramescitalopram oxalateEscitalopram oxalate 10 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-722
Escitalopramescitalopram oxalateEscitalopram oxalate 20 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-723
Escitalopramescitalopram oxalateEscitalopram oxalate 10 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0375

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