Cyclobenzaprine Hydrochloride NDC 85509-1920

Product information

Brand name (proprietary)

Cyclobenzaprine Hydrochloride

Generic name (nonproprietary)

cyclobenzaprine hydrochloride

Active ingredients

Cyclobenzaprine hydrochloride — 15 mg/1

Dosage form

Capsule, Extended release

Route

Oral

Labeler

PHOENIX RX LLC

Product type

Prescription drug

Marketing category

NDA authorized genericApplication NDA 021777

Marketing start

Mar 4, 2019

Listing expires

Dec 31, 2026

Other FDA classes

Centrally-mediated Muscle Relaxation (Physiologic effect)

Identifiers

Product ID 85509-1920_3a116427-c428-c3bc-e063-6294a90ac539SPL ID 3a116427-c428-c3bc-e063-6294a90ac539SPL set ID 3a116427-c427-c3bc-e063-6294a90ac539RxCUI 828358UNII 0VE05JYS2P

Pharmacologic class

Muscle Relaxant

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

N485509192003 followed by a unit qualifier and the quantity Copy

Package 85509-1920-03. 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 NDA 021777

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