Cyclobenzaprine Hydrochloride NDC 63187-590

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-590Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0590Add 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
63187-590-09	63187059009	9 TABLET, FILM COATED in 1 BOTTLE (63187-590-09)Marketed from May 13, 2026
63187-590-14	63187059014	14 TABLET, FILM COATED in 1 BOTTLE (63187-590-14)Marketed from Sep 4, 2024
63187-590-20	63187059020	20 TABLET, FILM COATED in 1 BOTTLE (63187-590-20)Marketed from Dec 1, 2018
63187-590-30	63187059030	30 TABLET, FILM COATED in 1 BOTTLE (63187-590-30)Marketed from Dec 1, 2018
63187-590-60	63187059060	60 TABLET, FILM COATED in 1 BOTTLE (63187-590-60)Marketed from Dec 1, 2018
63187-590-72	63187059072	120 TABLET, FILM COATED in 1 BOTTLE (63187-590-72)Marketed from Dec 1, 2018
63187-590-90	63187059090	90 TABLET, FILM COATED in 1 BOTTLE (63187-590-90)Marketed from Dec 1, 2018

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 Hydrochloride
Generic name (nonproprietary): cyclobenzaprine hydrochloride
Active ingredients: Cyclobenzaprine hydrochloride — 7.5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Proficient Rx LP
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078722
Marketing start: Mar 25, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 63187-590_dfd6a8bf-5460-47a3-9865-ec043cd9d17eSPL ID dfd6a8bf-5460-47a3-9865-ec043cd9d17eSPL set ID ae3a3f5c-fb64-4a43-be88-a2fc7c298ac1RxCUI 828299UNII 0VE05JYS2PUPC 0363187590307
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

N463187059009 followed by a unit qualifier and the quantity

Package 63187-0590-09. 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

Current FDA label (SPL), effective May 1, 2026.

Indications (excerpt from the label)

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 generally of short duration a…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078722

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

FDA NDC Directory listings under ANDA 078722
Product	Strength	Form · route	Labeler	Product NDC
Cyclobenzaprine Hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-1848
Cyclobenzaprine HCL	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	PHOENIX RX LLC	85509-1001
Cyclobenzaprine Hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Asclemed USA, Inc.	76420-010
Cyclobenzaprine Hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Direct_Rx	61919-261
Cyclobenzaprine Hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	SA3, LLC	69420-1001
Cyclobenzaprine HCL	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0078
Cyclobenzaprine Hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0096
Cyclobenzaprine Hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Quality Care Products LLC	55700-239
Cyclobenzaprine Hydrochloride	Cyclobenzaprine hydrochloride 7.5 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals, Inc.	68788-9967