NDC 55111-596

Memantine

Memantine

Memantine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Dr. Reddys Laboratories Limited. The primary component is Memantine Hydrochloride.

Product ID55111-596_0e1f7098-170b-68e7-eeeb-23fe6e51094c
NDC55111-596
Product TypeHuman Prescription Drug
Proprietary NameMemantine
Generic NameMemantine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-07-11
Marketing CategoryANDA / ANDA
Application NumberANDA090048
Labeler NameDr. Reddys Laboratories Limited
Substance NameMEMANTINE HYDROCHLORIDE
Active Ingredient Strength5 mg/1
Pharm ClassesNMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 55111-596-01

100 TABLET in 1 BOTTLE (55111-596-01)
Marketing Start Date2015-07-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 55111-596-78 [55111059678]

Memantine TABLET
Marketing CategoryANDA
Application NumberANDA090048
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-07-11

NDC 55111-596-30 [55111059630]

Memantine TABLET
Marketing CategoryANDA
Application NumberANDA090048
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-07-11

NDC 55111-596-05 [55111059605]

Memantine TABLET
Marketing CategoryANDA
Application NumberANDA090048
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-07-11

NDC 55111-596-60 [55111059660]

Memantine TABLET
Marketing CategoryANDA
Application NumberANDA090048
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-07-11

NDC 55111-596-79 [55111059679]

Memantine TABLET
Marketing CategoryANDA
Application NumberANDA090048
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-07-11

NDC 55111-596-01 [55111059601]

Memantine TABLET
Marketing CategoryANDA
Application NumberANDA090048
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-07-11

Drug Details

Active Ingredients

IngredientStrength
MEMANTINE HYDROCHLORIDE5 mg/1

OpenFDA Data

SPL SET ID:a71e2482-5266-d03e-8b36-862afe78c9a4
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 996561
  • 996571
    • UPC Code
  • 0355111596608

    • Pharmacological Class

    • NMDA Receptor Antagonists [MoA]
    • N-methyl-D-aspartate Receptor Antagonist [EPC]
    • NMDA Receptor Antagonists [MoA]
    • N-methyl-D-aspartate Receptor Antagonist [EPC]

    Medicade Reported Pricing

    55111059660 MEMANTINE HCL 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Memantine" or generic name "Memantine"

    NDCBrand NameGeneric Name
    0615-8100MemantineMemantine
    0615-8192MemantineMemantine
    0615-8319MemantineMemantine
    0904-6505MemantineMemantine
    0904-6506MemantineMemantine
    55111-596MemantineMemantine
    55111-597MemantineMemantine
    55154-4151MemantineMemantine
    55154-7637MemantineMemantine
    60505-6162MEMANTINEmemantine hydrochloride
    60687-173MemantineMemantine
    60687-184MemantineMemantine
    0378-1103Memantine Hydrochloridememantine
    0378-1104Memantine Hydrochloridememantine
    0378-5435Memantine Hydrochloridememantine
    0378-5436Memantine Hydrochloridememantine
    0378-5437Memantine Hydrochloridememantine
    0378-5438Memantine Hydrochloridememantine
    42291-551Memantine hydrochlorideMemantine
    42291-552Memantine hydrochlorideMemantine
    42292-005Memantine Hydrochloridememantine
    42292-006Memantine Hydrochloridememantine
    53746-169Memantine hydrochlorideMemantine
    53746-173Memantine hydrochlorideMemantine
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