What is NDC 80425-0155?

80425-0155 is the product NDC for Cyclobenzaprine HCL, Cyclobenzaprine hydrochloride 5 mg/1 tablet, film coated, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. It has 5 package NDCs, shown above in 10- and 11-digit form.

Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Cyclobenzaprine HCL?

6 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cyclobenzaprine HCL NDC 80425-0155

NDC codes

FDA NDC Directory

Product NDC (as listed)80425-0155Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80425-0155Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
80425-0155-1	8042501550180425015501	30 TABLET, FILM COATED in 1 BOTTLE (80425-0155-1)Marketed from Mar 30, 2023
80425-0155-2	8042501550280425015502	60 TABLET, FILM COATED in 1 BOTTLE (80425-0155-2)Marketed from Mar 30, 2023
80425-0155-3	8042501550380425015503	90 TABLET, FILM COATED in 1 BOTTLE (80425-0155-3)Marketed from Mar 30, 2023
80425-0155-4	8042501550480425015504	120 TABLET, FILM COATED in 1 BOTTLE (80425-0155-4)Marketed from Mar 30, 2023
80425-0155-5	8042501550580425015505	180 TABLET, FILM COATED in 1 BOTTLE (80425-0155-5)Marketed from Mar 30, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Cyclobenzaprine HCL
Generic name (nonproprietary): cyclobenzaprine hcl
Active ingredients: Cyclobenzaprine hydrochloride — 5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Advanced Rx Pharmacy of Tennessee, LLCNDC labeler code 80425
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213324
Marketing start: Jul 6, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 80425-0155_2a99a7c1-c4c1-2b01-e063-6294a90aa3b8SPL ID 2a99a7c1-c4c1-2b01-e063-6294a90aa3b8SPL set ID c859f63a-09de-4eec-e053-2a95a90a312fRxCUI 828320UNII 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

N480425015501 followed by a unit qualifier and the quantity

Package 80425-0155-01. 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

Current FDA label (SPL), effective Dec 31, 2024.

Indications (excerpt from the label)

Indications and Usage Section INDICATIONS AND USAGE Cyclobenzaprine hydrochloride tablets, USP are indicated as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions. Improvement is manifested by relief of muscle spasm and its associated signs and symptoms, namely, pain, tenderness, limitation of motion, and restriction in activities of daily living. Cyclobenzaprine hydrochloride tablets, USP should be used only for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use is not available and because muscle spasm associated with acute, painful musculoskeletal conditions is…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80425-0155

What is NDC 80425-0155?: 80425-0155 is the product NDC for Cyclobenzaprine HCL, Cyclobenzaprine hydrochloride 5 mg/1 tablet, film coated, listed with the FDA by Advanced Rx Pharmacy of Tennessee, LLC. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cyclobenzaprine HCL.
What is the active ingredient?: Cyclobenzaprine hydrochloride.
Who is the labeler?: Advanced Rx Pharmacy of Tennessee, LLC, NDC labeler code 80425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cyclobenzaprine HCL?: 6 other product NDCs are listed under this name. See all Cyclobenzaprine HCL NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Cyclobenzaprine HCL NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cyclobenzaprine HCL	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-680	72189-0680-3072189-0680-6072189-0680-90
Cyclobenzaprine HCL	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0016	80425-0016-0180425-0016-0280425-0016-03+1 more
Cyclobenzaprine HCL	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0018	80425-0018-0180425-0018-0280425-0018-03
Cyclobenzaprine HCL	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0078	80425-0078-0180425-0078-0280425-0078-03+1 more
Cyclobenzaprine HCL	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	PHOENIX RX LLC	85509-1001	85509-1001-0185509-1001-0385509-1001-06+1 more
Cyclobenzaprine HCL	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0017	80425-0017-01

Other NDCs under ANDA 213324

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

FDA NDC Directory listings under ANDA 213324
Product	Strength	Form · route	Labeler	Product NDC
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8508
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	Unichem Pharmaceuticals (USA), Inc.	29300-413
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Unichem Pharmaceuticals (USA), Inc.	29300-414
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	Unichem Pharmaceuticals (USA), Inc.	29300-415
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-5711
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-5712
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-5713
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-5756
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-5772
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-780
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	Redpharm Drug, Inc.	67296-1441
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-2471
Cyclobenzaprine Hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-3404
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-3567
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8637
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8706
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-3251
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 10 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-3702
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4265
Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-1961

Showing 20 of 30.