NDC codes

FDA NDC Directory
Product NDC (as listed)27241-071Labeler and product segments. Claims need a package NDC.
Product NDC at billing width27241-0071Add 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
27241-071-052724100710527241007105500 TABLET in 1 BOTTLE (27241-071-05)Marketed from Aug 27, 2015
27241-071-06272410071062724100710660 TABLET in 1 BOTTLE (27241-071-06)Marketed from Aug 27, 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 Hydrochloride
Generic name (nonproprietary)
memantine hydrochloride
Active ingredients
Memantine hydrochloride — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Ajanta Pharma USA Inc.NDC labeler code 27241
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206528
Marketing start
Listing expires
Other FDA classes
NMDA Receptor Antagonists (Mechanism)
Identifiers
Product ID 27241-071_078be4f6-c883-4178-be61-834fb9d5e4f5SPL ID 078be4f6-c883-4178-be61-834fb9d5e4f5SPL set ID 292671f2-f221-4a3d-a110-a266a9527e04RxCUI 996561, 996571UNII JY0WD0UA60UPC 0327241070068, 0327241071065
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

N427241007105 followed by a unit qualifier and the quantity

Package 27241-0071-05. 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 USP is indicated for the treatment of moderate to severe dementia of the Alzheimer’s type. Memantine hydrochloride USP 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 27241-071

What is NDC 27241-071?
27241-071 is the product NDC for Memantine Hydrochloride, Memantine hydrochloride 10 mg/1 tablet, listed with the FDA by Ajanta Pharma USA Inc.. It has 2 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?
Ajanta Pharma USA Inc., NDC labeler code 27241. 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 206528

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

FDA NDC Directory listings under ANDA 206528
ProductStrengthForm · routeLabelerProduct NDC
Memantine HCLMemantine hydrochloride 10 mg/1TabletOralDirect_Rx72189-538
Memantine HydrochlorideMemantine hydrochloride 5 mg/1TabletOralAjanta Pharma USA Inc.27241-070
Memantine HydrochlorideMemantine hydrochloride 10 mg/1TabletOralA-S Medication Solutions50090-6400
Memantine HydrochlorideMemantine hydrochloride 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8647
Memantine HydrochlorideMemantine hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-1899
Memantine HydrochlorideMemantine hydrochloride 10 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-885

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