NDC codes

FDA NDC Directory
Product NDC (as listed)60687-184Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0184Add 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
60687-184-57606870184576068701845760 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-184-57) / 1 TABLET in 1 BLISTER PACK (60687-184-11)Marketed from Sep 9, 2015

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)
Memantine
Generic name (nonproprietary)
memantine
Active ingredients
Memantine hydrochloride — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090048
Marketing start
Listing expires
Other FDA classes
NMDA Receptor Antagonists (Mechanism)
Identifiers
Product ID 60687-184_33621ba6-ed39-5bf8-e063-6394a90ab7e8SPL ID 33621ba6-ed39-5bf8-e063-6394a90ab7e8SPL set ID 304a3059-4f7f-4ec4-839d-86492bb5e07bRxCUI 996561, 996571UNII JY0WD0UA60
Pharmacologic class
N-methyl-D-aspartate Receptor Antagonist

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

N460687018457 followed by a unit qualifier and the quantity

Package 60687-0184-57. 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)

Memantine hydrochloride tablets are indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. Memantine hydrochloride is an N-methyl-D-aspartate (NMDA) receptor antagonist indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60687-184

What is NDC 60687-184?
60687-184 is the product NDC for Memantine, Memantine hydrochloride 10 mg/1 tablet, 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?
Memantine.
What is the active ingredient?
Memantine 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 Memantine?
8 other product NDCs are listed under this name. See all Memantine 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 Memantine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
MemantineMemantine hydrochloride 5 mg/1TabletOralNorthStar RxLLC72603-11872603-0118-01
MemantineMemantine hydrochloride 10 mg/1TabletOralNorthStar RxLLC72603-11972603-0119-0172603-0119-02
memantineMemantine hydrochloride 5 mg/1TabletOralChartwell RX, LLC62135-89562135-0895-60
memantineMemantine hydrochloride 10 mg/1TabletOralChartwell RX, LLC62135-89662135-0896-60
Memantinememantine hydrochlorideMemantine hydrochloride 2 mg/mLSolutionOralApotex Corp.60505-616260505-6162-05
MemantineMemantine hydrochloride 5 mg/1TabletOralAmerican Health Packaging60687-17360687-0173-57
MemantineMemantine hydrochloride 5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-819200615-8192-39
MemantineMemantine hydrochloride 10 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-831900615-8319-0500615-8319-39

Other NDCs under ANDA 090048

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

FDA NDC Directory listings under ANDA 090048
ProductStrengthForm · routeLabelerProduct NDC
MemantineMemantine hydrochloride 5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8192
MemantineMemantine hydrochloride 10 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8319
MemantineMemantine hydrochloride 5 mg/1TabletOralAmerican Health Packaging60687-173
MemantineMemantine hydrochloride 5 mg/1TabletOralNorthStar RxLLC72603-118
MemantineMemantine hydrochloride 10 mg/1TabletOralNorthStar RxLLC72603-119
Memantine HydrochlorideMemantine hydrochloride 5 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6505
Memantine HydrochlorideMemantine hydrochloride 10 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-6506
Memantine HydrochlorideMemantine hydrochloride 5 mg/1Tablet, Film coatedOralDr. Reddys Laboratories Limited55111-596
Memantine HydrochlorideMemantine hydrochloride 10 mg/1Tablet, Film coatedOralDr. Reddys Laboratories Limited55111-597
Memantine HydrochlorideMemantine hydrochloride 5 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-4151
Memantine HydrochlorideMemantine hydrochloride 10 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-7637

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