Quetiapine Fumarate NDC 68071-3931

Product information

Brand name (proprietary)

Quetiapine Fumarate

Generic name (nonproprietary)

quetiapine fumarate

Active ingredients

Quetiapine fumarate — 25 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

NuCare Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

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

Marketing start

Jul 1, 2016

Listing expires

Dec 31, 2026

Identifiers

Product ID 68071-3931_458cae68-c11e-e760-e063-6394a90ac04eSPL ID 458cae68-c11e-e760-e063-6394a90ac04eSPL set ID 458cae68-c11d-e760-e063-6394a90ac04eRxCUI 312744UNII 2S3PL1B6UJUPC 0368071393194

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

N468071393109 followed by a unit qualifier and the quantity Copy

Package 68071-3931-09. 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 202674

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