Oxycodone Hydrochloride NDC 55700-174

Product information

Brand name (proprietary)

Oxycodone Hydrochloride

Generic name (nonproprietary)

oxycodone hydrochloride

Active ingredients

Oxycodone hydrochloride — 15 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Quality Care Products LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 091393

Marketing start

Oct 18, 2013

Marketing end

Jul 31, 2027

DEA schedule

CII

Other FDA classes

Full Opioid Agonists (Mechanism)

Identifiers

Product ID 55700-174_dd30b87d-7f9b-43b8-b32e-c4d2937d6931SPL ID dd30b87d-7f9b-43b8-b32e-c4d2937d6931SPL set ID 4cadb809-157d-49cc-97b4-3276594f19d2RxCUI 1049611, 1049618UNII C1ENJ2TE6C

Pharmacologic class

Opioid Agonist

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

N455700017430 followed by a unit qualifier and the quantity Copy

Package 55700-0174-30. 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

Other NDCs under ANDA 091393

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