NDC codes

FDA NDC Directory
Product NDC (as listed)69097-845Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69097-0845Add 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 NDC11-digit (billing)PackageCopy
69097-845-0769097084507100 TABLET, FILM COATED in 1 BOTTLE (69097-845-07)Marketed from Jul 22, 2016
69097-845-15690970845151000 TABLET, FILM COATED in 1 BOTTLE (69097-845-15)Marketed from Jul 22, 2016

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
Active ingredients
Cyclobenzaprine hydrochloride — 5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090478
Marketing start
Listing expires
Other FDA classes
Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers
Product ID 69097-845_e41dbd69-00e7-40f4-a9e7-626965badd27SPL ID e41dbd69-00e7-40f4-a9e7-626965badd27SPL set ID 575a31fb-04c5-4001-88a7-c33adbacc6a8RxCUI 828320, 828348UNII 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

N469097084507 followed by a unit qualifier and the quantity

Package 69097-0845-07. 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 090478

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

FDA NDC Directory listings under ANDA 090478
ProductStrengthForm · routeLabelerProduct NDC
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-558
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-973
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3150
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals, Inc.68071-3154
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8084
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1TabletOralEXELAN PHARMACEUTICALS, INC.76282-283
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1Tablet, Film coatedOralCipla USA Inc.69097-846
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1Tablet, Film coatedOralProficient Rx LP63187-812
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-933
Cyclobenzaprine HydrochlorideCyclobenzaprine hydrochloride 5 mg/1Tablet, Film coatedOralAvPAK50268-190
Cyclobenzaprine HydrochloridecyclobenzaprineCyclobenzaprine hydrochloride 10 mg/1Tablet, Film coatedOralAvPAK50268-191

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