Methadone Hydrochloride NDC 60687-910

NDC codes

FDA NDC Directory

Product NDC (as listed)60687-910Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60687-0910Add 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
60687-910-01	60687091001	100 BLISTER PACK in 1 CARTON (60687-910-01) / 1 TABLET in 1 BLISTER PACK (60687-910-11)Marketed from Sep 9, 2026

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): Methadone Hydrochloride
Generic name (nonproprietary): methadone hydrochloride
Active ingredients: Methadone hydrochloride — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: American Health Packaging
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211228
Marketing start: Sep 9, 2026
Listing expires: Dec 31, 2027
DEA schedule: CII
Other FDA classes: Full Opioid Agonists (Mechanism)
Identifiers: Product ID 60687-910_5b1344a0-2ae2-1751-e063-6394a90a46feSPL ID 5b1344a0-2ae2-1751-e063-6394a90a46feSPL set ID 540edd43-165d-4257-b989-3bccc8f54afbRxCUI 864706UNII 229809935B
Pharmacologic class: Opioid 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

N460687091001 followed by a unit qualifier and the quantity

Package 60687-0910-01. 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 Sep 9, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Methadone hydrochloride tablets are indicated for the: 1. Management of severe and persistent pain that requires an opioid analgesic and that cannot be adequately treated with alternative options, including immediate-release opioids. Limitations of Use Because of the risks of addiction, abuse, misuse, overdose, and death, which can occur at any dosage or duration [see Warnings and Precautions (5.1) ] and persist over the course of therapy, reserve opioid analgesics, including methadone hydrochloride tablets, for use in patients for whom alternative treatment options are ineffective, not tolerated, or would be otherwise inadequate to provide sufficient management of pain. Methadone hydrochlor…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211228

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

FDA NDC Directory listings under ANDA 211228
Product	Strength	Form · route	Labeler	Product NDC
Methadone Hydrochloride	Methadone hydrochloride 5 mg/1	TabletOral	XLCare Pharmaceuticals, Inc	72865-120
Methadone Hydrochloride	Methadone hydrochloride 10 mg/1	TabletOral	XLCare Pharmaceuticals, Inc	72865-121
Methadone Hydrochloride	Methadone hydrochloride 5 mg/1	TabletOral	Camber Pharmaceuticals, Inc	31722-946
Methadone Hydrochloride	Methadone hydrochloride 10 mg/1	TabletOral	Camber Pharmaceuticals, Inc	31722-947