Prescription drug · ANDA

Escitalopram Oxalate NDC 72603-149

Escitalopram oxalate 5 mg/1 · Tablet, Film coated · Oral · NorthStar RxLLC

NDC codes

FDA NDC Directory
Product NDC (as listed)72603-149Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72603-0149Add 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
72603-149-01726030149011000 TABLET, FILM COATED in 1 BOTTLE (72603-149-01)Marketed from Jan 8, 2024

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 Oxalate
Generic name (nonproprietary)
escitalopram oxalate
Active ingredients
Escitalopram oxalate — 5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202210
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 72603-149_cb888b2f-8092-43a1-8542-a10e2b004369SPL ID cb888b2f-8092-43a1-8542-a10e2b004369SPL set ID 81840aec-96fd-4af2-bd10-3f38d068f39aRxCUI 349332, 351249, 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

N472603014901 followed by a unit qualifier and the quantity

Package 72603-0149-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 202210

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

FDA NDC Directory listings under ANDA 202210
ProductStrengthForm · routeLabelerProduct NDC
Escitalopram OxalateEscitalopram oxalate 20 mg/21Tablet, Film coatedOralA-S Medication Solutions50090-7200
Escitalopram OxalateEscitalopram oxalate 20 mg/21Tablet, Film coatedOralA-S Medication Solutions50090-7201
Escitalopram OxalateEscitalopram oxalate 10 mg/21Tablet, Film coatedOralNorthStar RxLLC72603-150
Escitalopram OxalateEscitalopram oxalate 20 mg/21Tablet, Film coatedOralNorthStar RxLLC72603-151
Escitalopram OxalateEscitalopram oxalate 5 mg/1Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-036
Escitalopram OxalateEscitalopram oxalate 10 mg/21Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-037
Escitalopram OxalateEscitalopram oxalate 20 mg/21Tablet, Film coatedOralMacleods Pharmaceuticals Limited33342-038

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