Guanfacine NDC 70518-4488

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4488Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4488Add 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	Copy
70518-4488-0	70518448800	30 TABLET in 1 BLISTER PACK (70518-4488-0)Marketed from Sep 30, 2025

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): Guanfacine
Generic name (nonproprietary): guanfacine
Active ingredients: Guanfacine hydrochloride — 2 mg/1
Dosage form: Tablet
Route: Oral
Labeler: REMEDYREPACK INC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217293
Marketing start: Sep 30, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha2-Agonists (Mechanism)
Identifiers: Product ID 70518-4488_5b71bf5c-e0d2-b0fe-e063-6394a90afc8dSPL ID 5b71bf5c-e0d2-b0fe-e063-6394a90afc8d
Pharmacologic class: Central alpha-2 Adrenergic Agonist

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

N470518448800 followed by a unit qualifier and the quantity

Package 70518-4488-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 217293

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

FDA NDC Directory listings under ANDA 217293
Product	Strength	Form · route	Labeler	Product NDC
Guanfacine	Guanfacine hydrochloride 2 mg/1	TabletOral	Coupler LLC	67046-1655
Guanfacine	Guanfacine hydrochloride 1 mg/1	TabletOral	Coupler LLC	67046-1433
Guanfacine	Guanfacine hydrochloride 1 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-242
Guanfacine	Guanfacine hydrochloride 2 mg/1	TabletOral	Ajanta Pharma USA Inc.	27241-243
Guanfacine	Guanfacine hydrochloride 1 mg/1	TabletOral	REMEDYREPACK INC.	70518-4333