Quetiapine Fumarate NDC 67046-1649

Product information

Brand name (proprietary)

Quetiapine Fumarate

Generic name (nonproprietary)

quetiapine fumarate

Active ingredients

Quetiapine fumarate — 50 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Coupler LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 202674

Marketing start

Jan 15, 2026

Listing expires

Dec 31, 2027

Identifiers

Product ID 67046-1649_48727af1-1bd2-125a-e063-6394a90a7150SPL ID 48727af1-1bd2-125a-e063-6394a90a7150SPL set ID 4872793c-a7be-1b65-e063-6394a90a8b3aRxCUI 616487UNII 2S3PL1B6UJ

Pharmacologic class

Atypical Antipsychotic

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

N467046164903 followed by a unit qualifier and the quantity Copy

Package 67046-1649-03. 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 202674

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