NDC codes

FDA NDC Directory
Product NDC (as listed)65162-783Labeler and product segments. Claims need a package NDC.
Product NDC at billing width65162-0783Add 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
65162-783-03651620783036516207830330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-783-03)Marketed from Dec 22, 2017
65162-783-09651620783096516207830990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-783-09)Marketed from Dec 22, 2017
65162-783-506516207835065162078350500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65162-783-50)Marketed from Dec 22, 2017

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 Hydrochloride
Generic name (nonproprietary)
memantine hydrochloride
Active ingredients
Memantine hydrochloride — 14 mg/1
Dosage form
Capsule, Extended release
Route
Oral
Labeler
Amneal Pharmaceuticals LLCNDC labeler code 65162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205825
Marketing start
Listing expires
Other FDA classes
NMDA Receptor Antagonists (Mechanism)
Identifiers
Product ID 65162-783_fb7782a5-2357-4a21-86a6-0eeaa7cdcea5SPL ID fb7782a5-2357-4a21-86a6-0eeaa7cdcea5SPL set ID f2b7538d-8ca1-4ac7-a172-d268e2fa9a52RxCUI 996594, 996603, 996609, 996615UNII JY0WD0UA60UPC 0365162784091, 0365162783094, 0365162785098, 0365162782097
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

N465162078303 followed by a unit qualifier and the quantity

Package 65162-0783-03. 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)

Memantine hydrochloride extended-release capsules are indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. Memantine hydrochloride extended-release capsules are a 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 65162-783

What is NDC 65162-783?
65162-783 is the product NDC for Memantine Hydrochloride, Memantine hydrochloride 14 mg/1 capsule, extended release, listed with the FDA by Amneal Pharmaceuticals LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Memantine Hydrochloride.
What is the active ingredient?
Memantine hydrochloride.
Who is the labeler?
Amneal Pharmaceuticals LLC, NDC labeler code 65162. 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 Hydrochloride?
111 other product NDCs are listed under this name. See all Memantine 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 Memantine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Memantine hydrochlorideMemantine hydrochloride 7 mg/1Capsule, Extended releaseOralMacleods Pharmaceuticals Limited33342-21933342-0219-0733342-0219-12
Memantine hydrochlorideMemantine hydrochloride 14 mg/1Capsule, Extended releaseOralMacleods Pharmaceuticals Limited33342-22033342-0220-0733342-0220-12
Memantine hydrochlorideMemantine hydrochloride 21 mg/1Capsule, Extended releaseOralMacleods Pharmaceuticals Limited33342-22133342-0221-0733342-0221-12
Memantine hydrochlorideMemantine hydrochloride 28 mg/1Capsule, Extended releaseOralMacleods Pharmaceuticals Limited33342-22233342-0222-0733342-0222-12
Memantine HydrochlorideMemantine hydrochloride 5 mg/1Tablet, Film coatedOralCarlsbad Technology, Inc.61442-19261442-0192-0561442-0192-60
Memantine HydrochlorideMemantine hydrochloride 10 mg/1Tablet, Film coatedOralCarlsbad Technology, Inc.61442-19361442-0193-0561442-0193-60
Memantine HydrochloridememantineMemantine hydrochloride 7 mg/1Capsule, Extended releaseOralRising Pharma Holdings, Inc.16571-85216571-0852-03
Memantine HydrochloridememantineMemantine hydrochloride 14 mg/1Capsule, Extended releaseOralRising Pharma Holdings, Inc.16571-85316571-0853-0316571-0853-09
Memantine HydrochloridememantineMemantine hydrochloride 21 mg/1Capsule, Extended releaseOralRising Pharma Holdings, Inc.16571-85416571-0854-03
Memantine HydrochloridememantineMemantine hydrochloride 28 mg/1Capsule, Extended releaseOralRising Pharma Holdings, Inc.16571-85516571-0855-0316571-0855-09

All 112 Memantine Hydrochloride NDCs

Other NDCs under ANDA 205825

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

FDA NDC Directory listings under ANDA 205825
ProductStrengthForm · routeLabelerProduct NDC
Memantine HydrochlorideMemantine hydrochloride 7 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals LLC65162-782
Memantine HydrochlorideMemantine hydrochloride 21 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals LLC65162-784
Memantine HydrochlorideMemantine hydrochloride 28 mg/1Capsule, Extended releaseOralAmneal Pharmaceuticals LLC65162-785

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