Package 71335-1732-2

Brand: memantine hydrochloride

Generic: memantine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1732-2
Digits Only 7133517322
Product NDC 71335-1732
Description

60 TABLET in 1 BOTTLE (71335-1732-2)

Marketing

Marketing Status
Marketed Since 2020-11-11
Brand memantine hydrochloride
Generic memantine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "216899e3-38c6-4ac6-9ffc-ec5264ef4246", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996571"], "spl_set_id": ["9cfddd01-6e1d-4ee0-9310-3fb371724e3d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1732-1)", "package_ndc": "71335-1732-1", "marketing_start_date": "20201111"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1732-2)", "package_ndc": "71335-1732-2", "marketing_start_date": "20201111"}], "brand_name": "Memantine Hydrochloride", "product_id": "71335-1732_216899e3-38c6-4ac6-9ffc-ec5264ef4246", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "71335-1732", "generic_name": "Memantine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine Hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090961", "marketing_category": "ANDA", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}