NDC codes

FDA NDC Directory
Product NDC (as listed)17856-1927Labeler and product segments. Claims need a package NDC.
Product NDC at billing width17856-1927Add 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
17856-1927-717856192707178561927071 SYRINGE in 1 BAG (17856-1927-7) / .5 mL in 1 SYRINGEMarketed from May 29, 2025
17856-1927-817856192708178561927081 SYRINGE in 1 BAG (17856-1927-8) / 1 mL in 1 SYRINGEMarketed from May 29, 2025
17856-1927-917856192709178561927091 SYRINGE in 1 BAG (17856-1927-9) / 2.5 mL in 1 SYRINGEMarketed from May 29, 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)
Methadone Hydrocloride dye-free, sugar-free, unflavoredSuffix: dye-free, sugar-free, unflavored
Generic name (nonproprietary)
methadone hydrochloride
Active ingredients
Methadone hydrochloride — 10 mg/mL
Dosage form
Concentrate
Route
Oral
Labeler
Atlantic Biologicals Corp.NDC labeler code 17856
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212093
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Full Opioid Agonists (Mechanism)
Identifiers
Product ID 17856-1927_373c6844-095b-a726-e063-6294a90a2544SPL ID 373c6844-095b-a726-e063-6294a90a2544SPL set ID 373c649e-798d-770e-e063-6294a90a6e47RxCUI 991147UNII 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

N417856192707 followed by a unit qualifier and the quantity

Package 17856-1927-07. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Methadone Hydrochloride contains methadone, an opioid agonist indicated for the: detoxification treatment of opioid addiction (heroin or other morphine-like drugs). maintenance treatment of opioid addiction (heroin or other morphine-like drugs), in conjunction with appropriate social and medical services. Limitations of Use Methadone products used for the treatment of opioid addiction in detoxification or maintenance programs are subject to the conditions for distribution and use required under 21 CFR, Title 42, Sec 8 [see Dosage and Administration ( 2.1 )] . Methadone Hydrochloride is an opioid agonist indicated for the: Detoxification treatment of opioid addiction (heroin or other morphine…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17856-1927

What is NDC 17856-1927?
17856-1927 is the product NDC for Methadone Hydrocloride dye-free, sugar-free, unflavored, Methadone hydrochloride 10 mg/mL concentrate, listed with the FDA by Atlantic Biologicals Corp.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Methadone Hydrocloride dye-free, sugar-free, unflavored (Methadone hydrochloride).
What is the active ingredient?
Methadone hydrochloride.
Who is the labeler?
Atlantic Biologicals Corp., NDC labeler code 17856. 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 Hydrocloride dye-free, sugar-free, unflavored?
3 other product NDCs are listed under this name. See all Methadone Hydrocloride dye-free, sugar-free, unflavored 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 Hydrocloride dye-free, sugar-free, unflavored NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Methadone Hydrocloride dye-free, sugar-free, unflavoredmethadone hydrochlorideMethadone hydrochloride 10 mg/mLConcentrateOralLannett Company, Inc.0527-192700527-1927-3600527-1927-39
Methadone Hydrocloride dye-free, sugar-free, unflavoredmethadone hydrochlorideMethadone hydrochloride 10 mg/mLConcentrateOralBryant Ranch Prepack63629-209863629-2098-01
Methadone Hydrocloride dye-free, sugar-free, unflavoredmethadone hydrochlorideMethadone hydrochloride 10 mg/mLConcentrateOralBryant Ranch Prepack72162-108572162-1085-02

Other NDCs under ANDA 212093

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

FDA NDC Directory listings under ANDA 212093
ProductStrengthForm · routeLabelerProduct NDC
Methadone Hydrocloride dye-free, sugar-free, unflavoredmethadone hydrochlorideMethadone hydrochloride 10 mg/mLConcentrateOralLannett Company, Inc.0527-1927
Methadone Hydrocloride dye-free, sugar-free, unflavoredmethadone hydrochlorideMethadone hydrochloride 10 mg/mLConcentrateOralBryant Ranch Prepack63629-2098
Methadone Hydrocloride dye-free, sugar-free, unflavoredmethadone hydrochlorideMethadone hydrochloride 10 mg/mLConcentrateOralBryant Ranch Prepack72162-1085

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