NDC codes

FDA NDC Directory
Product NDC (as listed)60687-818Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0818Add 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
60687-818-8660687081886606870818863 TRAY in 1 CASE (60687-818-86) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-818-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-818-40)Marketed from Dec 16, 2024

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 — 5 mg/5mL
Dosage form
Solution
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 087393
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 60687-818_3506271d-27f4-2065-e063-6394a90ac386SPL ID 3506271d-27f4-2065-e063-6394a90ac386SPL set ID f935effe-e5b2-4bf7-bbde-6e80bb99076fRxCUI 864761UNII 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

N460687081886 followed by a unit qualifier and the quantity

Package 60687-0818-86. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Methadone Hydrochloride Oral Solution is indicated for the: Management of severe and persistent pain that requires an extended treatment period with a daily opioid analgesic and for which alternative treatment options are inadequate. Limitations of Use: Because of the risks of addiction, abuse, and misuse with opioids, which can occur at any dosage or duration [see Warnings and Precautions (5.2)], reserve Methadone Hydrochloride Oral Solution for use in patients for whom alternative analgesic treatment options (e.g., non-opioid analgesics or opioid combination products): Have not been tolerated or are not expected to be tolerated, Have not provided adequate analgesia or are not expected to p…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-818

What is NDC 60687-818?
60687-818 is the product NDC for Methadone Hydrochloride, Methadone hydrochloride 5 mg/5mL solution, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Methadone Hydrochloride.
What is the active ingredient?
Methadone hydrochloride.
Who is the labeler?
American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Methadone Hydrochloride?
41 other product NDCs are listed under this name. See all Methadone Hydrochloride NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Methadone Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Methadone HydrochlorideMethadone hydrochloride 10 mg/1TabletOralAmerican Health Packaging60687-91060687-0910-01
Methadone HydrochlorideMethadone hydrochloride 5 mg/1TabletOralAscend Laboratories, LLC67877-65967877-0659-01
Methadone HydrochlorideMethadone hydrochloride 10 mg/1TabletOralAscend Laboratories, LLC67877-66067877-0660-01
Methadone HydrochlorideMethadone hydrochloride 200 mg/20mLInjectionIntravenousLong Grove Pharmaceuticals, LLC81298-750081298-7500-01
Methadone HydrochlorideMethadone hydrochloride 10 mg/mLInjectionIntramuscular, Intravenous, SubcutaneousHikma Pharmaceuticals USA Inc.0641-626600641-6266-01
Methadone HydrochlorideMethadone hydrochloride 10 mg/mLInjection, SolutionIntramuscular, Intravenous, SubcutaneousBreckenridge Pharmaceutical Inc51991-00251991-0002-98
Methadone HydrochlorideMethadone hydrochloride 10 mg/1TabletOralMajor Pharmaceuticals0904-741700904-7417-61
Methadone HydrochlorideMethadone hydrochloride 5 mg/5mLSolutionOralPrecision Dose, Inc.68094-33168094-0331-58
Methadone HydrochlorideMethadone hydrochloride 10 mg/mLConcentrateOralSpecGx LLC0406-412300406-4123-0300406-4123-10
Methadone HydrochlorideMethadone hydrochloride 10 mg/5mLSolutionOralSpecGx LLC0406-622100406-6221-05

All 42 Methadone Hydrochloride NDCs

Other NDCs under ANDA 087393

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

FDA NDC Directory listings under ANDA 087393
ProductStrengthForm · routeLabelerProduct NDC
Methadone HydrochlorideMethadone hydrochloride 5 mg/5mLSolutionOralHikma Pharmaceuticals USA Inc.0054-3555
Methadone HydrochlorideMethadone hydrochloride 5 mg/5mLSolutionOralPrecision Dose, Inc.68094-031
Methadone HydrochlorideMethadone hydrochloride 5 mg/5mLSolutionOralPrecision Dose, Inc.68094-331

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