Levothyroxine sodium NDC 68071-3619

Product information

Brand name (proprietary)

Levothyroxine sodium

Generic name (nonproprietary)

levothyroxine sodium

Active ingredients

Levothyroxine sodium — 200 ug/1

Dosage form

Tablet

Route

Oral

Labeler

NuCare Pharmaceuticals,Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 212399

Marketing start

Dec 3, 2020

Listing expires

Dec 31, 2026

Other FDA classes

Thyroxine (Chemical structure)

Identifiers

Product ID 68071-3619_1ac85666-6200-3887-e063-6394a90a105eSPL ID 1ac85666-6200-3887-e063-6394a90a105eSPL set ID 1ac856d1-7067-a71d-e063-6294a90acc7cRxCUI 892251UNII 9J765S329GUPC 0368071361995

Pharmacologic class

l-Thyroxine

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

N468071361909 followed by a unit qualifier and the quantity Copy

Package 68071-3619-09. 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 212399

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

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