NDC codes

FDA NDC Directory
Product NDC (as listed)67046-1452Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67046-1452Add 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
67046-1452-3670461452036704614520330 TABLET in 1 BLISTER PACK (67046-1452-3)Marketed from Feb 7, 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)
Amantadine Hydrochloride
Generic name (nonproprietary)
amantadine hydrochloride
Active ingredients
Amantadine hydrochloride — 100 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Coupler LLCNDC labeler code 67046
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209035
Marketing start
Listing expires
Other FDA classes
M2 Protein Inhibitors (Mechanism)
Identifiers
Product ID 67046-1452_2d940d35-6a65-e494-e063-6394a90a9d16SPL ID 2d940d35-6a65-e494-e063-6394a90a9d16SPL set ID 2d94073b-c064-c280-e063-6294a90af145RxCUI 849395UNII M6Q1EO9TD0
Pharmacologic class
Influenza A M2 Protein Inhibitor

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

N467046145203 followed by a unit qualifier and the quantity

Package 67046-1452-03. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Amantadine Hydrochloride Tablets are indicated for the prophylaxis and treatment of signs and symptoms of infection caused by various strains of influenza A virus. Amantadine Hydrochloride Tablets are also indicated in the treatment of parkinsonism and drug-induced extrapyramidal reactions. Influenza A Prophylaxis Amantadine Hydrochloride Tablets are indicated for chemoprophylaxis against signs and symptoms of influenza A virus infection. Because Amantadine Hydrochloride Tablets do not completely prevent the host immune response to influenza A infection, individuals who take this drug may still develop immune responses to natural disease or vaccination and may be protec…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67046-1452

What is NDC 67046-1452?
67046-1452 is the product NDC for Amantadine Hydrochloride, Amantadine hydrochloride 100 mg/1 tablet, listed with the FDA by Coupler LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Amantadine Hydrochloride.
What is the active ingredient?
Amantadine hydrochloride.
Who is the labeler?
Coupler LLC, NDC labeler code 67046. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Amantadine Hydrochloride?
40 other product NDCs are listed under this name. See all Amantadine 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 Amantadine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
amantadine hydrochlorideAmantadine hydrochloride 100 mg/1CapsuleOralAvKARE73190-09473190-0094-50
Amantadine HydrochlorideAmantadine hydrochloride 50 mg/5mLSolutionOralBAJAJ MEDICAL, LLC61037-48461037-0484-03
amantadine hydrochlorideAmantadine hydrochloride 100 mg/1CapsuleOralCoupler LLC67046-150867046-1508-03
Amantadine HydrochlorideAmantadine hydrochloride 100 mg/1TabletOralZhejiang Jutai Pharmaceutical Co., Ltd.71765-00971765-0009-01
Amantadine HydrochlorideAmantadine hydrochloride 50 mg/5mLSolutionOralAmerican Health Packaging60687-79760687-0797-56
Amantadine HydrochlorideAmantadine hydrochloride 50 mg/5mLSolutionOralPatrin Pharma, Inc.39328-53039328-0530-1639328-0530-99
Amantadine HydrochlorideAmantadine hydrochloride 100 mg/1Capsule, Liquid filledOralStrides Pharma Science Limited64380-86264380-0862-0664380-0862-07
Amantadine HydrochlorideAmantadine hydrochloride 100 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-83416571-0834-0116571-0834-50
amantadine hydrochlorideAmantadine hydrochloride 100 mg/1CapsuleOralEPIC PHARMA LLC42806-71642806-0716-0542806-0716-11
Amantadine HydrochlorideAmantadine hydrochloride 100 mg/1CapsuleOralST. MARY'S MEDICAL PARK PHARMACY60760-77960760-0779-30

All 41 Amantadine Hydrochloride NDCs

Other NDCs under ANDA 209035

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

FDA NDC Directory listings under ANDA 209035
ProductStrengthForm · routeLabelerProduct NDC
Amantadine HCLAmantadine hydrochloride 100 mg/1TabletOralDirect_Rx72189-535
Amantadine HydrochlorideAmantadine hydrochloride 100 mg/1TabletOralStrides Pharma Inc.42543-497

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