Memantine Hydrochloride NDC 71335-1732

Product information

Brand name (proprietary)

Memantine Hydrochloride

Generic name (nonproprietary)

memantine hydrochloride

Active ingredients

Memantine hydrochloride — 5 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 71335-1732_216899e3-38c6-4ac6-9ffc-ec5264ef4246SPL ID 216899e3-38c6-4ac6-9ffc-ec5264ef4246SPL set ID 9cfddd01-6e1d-4ee0-9310-3fb371724e3dRxCUI 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

N471335173201 followed by a unit qualifier and the quantity Copy

Package 71335-1732-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 090961

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