What is NDC 70792-102?

70792-102 is the product NDC for Tonmya (cyclobenzaprine hydrochloride), Cyclobenzaprine hydrochloride 2.8 mg/1 tablet, orally disintegrating, listed with the FDA by Tonix Medicines, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Tonmya (Cyclobenzaprine Hydrochloride).

Tonix Medicines, Inc., NDC labeler code 70792. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Tonmya?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Tonmya NDC 70792-102 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70792-102Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70792-0102Add 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
70792-102-14	7079201021470792010214	14 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (70792-102-14)Marketed from Sep 15, 2025
70792-102-30	7079201023070792010230	30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (70792-102-30)Marketed from Oct 23, 2025
70792-102-60	7079201026070792010260	60 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (70792-102-60)Marketed from Sep 15, 2025
70792-102-90	7079201029070792010290	90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (70792-102-90)Marketed from Sep 15, 2025

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): Tonmya
Generic name (nonproprietary): cyclobenzaprine hydrochloride
Active ingredients: Cyclobenzaprine hydrochloride — 2.8 mg/1
Dosage form: Tablet, Orally disintegrating
Route: Sublingual
Labeler: Tonix Medicines, Inc.NDC labeler code 70792
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 219428
Marketing start: Aug 15, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Centrally-mediated Muscle Relaxation (Physiologic effect)
Identifiers: Product ID 70792-102_c3457853-101e-46ee-899a-1f7539017eabSPL ID c3457853-101e-46ee-899a-1f7539017eabSPL set ID 6fa59588-ce9b-48cf-8c5f-725a448f8571RxCUI 2723106, 2723114UNII 0VE05JYS2PUPC 0370792102306
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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470792010214 followed by a unit qualifier and the quantity

Package 70792-0102-14. 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 Aug 14, 2026.

Indications (excerpt from the label)

TONMYA ® is indicated for treatment of fibromyalgia in adults. TONMYA is indicated for the treatment of fibromyalgia in adults ( 1 ).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70792-102

What is NDC 70792-102?: 70792-102 is the product NDC for Tonmya (cyclobenzaprine hydrochloride), Cyclobenzaprine hydrochloride 2.8 mg/1 tablet, orally disintegrating, listed with the FDA by Tonix Medicines, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Tonmya (Cyclobenzaprine Hydrochloride).
What is the active ingredient?: Cyclobenzaprine hydrochloride.
Who is the labeler?: Tonix Medicines, Inc., NDC labeler code 70792. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Tonmya?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Tonmya (Cyclobenzaprine hydrochloride) NDC 70792-102