Memantine Hydrochloride NDC 71335-1603

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

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 090961

Marketing start

Feb 28, 2019

Listing expires

Dec 31, 2026

Other FDA classes

NMDA Receptor Antagonists (Mechanism)

Identifiers

Product ID 71335-1603_7a5a4451-bd05-4f77-9c6c-563119465803SPL ID 7a5a4451-bd05-4f77-9c6c-563119465803SPL set ID bf395152-2885-4633-bf3f-2da46e7b79f1RxCUI 996561UNII 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

N471335160301 followed by a unit qualifier and the quantity Copy

Package 71335-1603-01. 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

Other NDCs under ANDA 090961

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