Prescription drug · ANDA

Escitalopram NDC 42708-163

Escitalopram oxalate 20 mg/1 · Tablet, Film coated · Oral · QPharma, Inc.

NDC codes

FDA NDC Directory
Product NDC (as listed)42708-163Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42708-0163Add 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
42708-163-304270801633030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-163-30)Marketed from Mar 13, 2023 · Sample package

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 — 20 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
QPharma, Inc.NDC labeler code 42708
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 42708-163_4586cb37-a5df-2caf-e063-6294a90a48c6SPL ID 4586cb37-a5df-2caf-e063-6294a90a48c6SPL set ID f682f991-1807-176a-e053-2995a90a3dfaRxCUI 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

N442708016330 followed by a unit qualifier and the quantity

Package 42708-0163-30. 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 . 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 42708-163

What is NDC 42708-163?
42708-163 is the product NDC for Escitalopram, Escitalopram oxalate 20 mg/1 tablet, film coated, listed with the FDA by QPharma, Inc.. 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?
QPharma, Inc., NDC labeler code 42708. 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 coatedOralProficient Rx LP71205-782
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1241
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1307
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralQPharma, Inc.42708-155
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5312
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralCoupler LLC67046-0355
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0320
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-865
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralDirect_Rx72189-424
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-116
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralDirect_Rx72189-449
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralDirect_Rx72189-451
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2317
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc.68788-7461
EscitalopramEscitalopram oxalate 5 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-591
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5248
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-592
EscitalopramEscitalopram oxalate 20 mg/1Tablet, Film coatedOralBluePoint Laboratories68001-593
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4567
EscitalopramEscitalopram oxalate 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2472

Showing 20 of 32.

Med-Code uses cookies for analytics and advertising. You can accept or reject them; the site works either way. Privacy Policy.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in