Package 68180-248-06
Brand: memantine hydrochloride
Generic: memantine hydrochloridePackage Facts
Identity
Package NDC
68180-248-06
Digits Only
6818024806
Product NDC
68180-248
Description
30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68180-248-06)
Marketing
Marketing Status
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": "2eba035e-38ce-479d-8dc8-0bfdd2bffbcf", "openfda": {"upc": ["0368180247067", "0368180249061", "0368180246060"], "unii": ["JY0WD0UA60"], "rxcui": ["996594", "996603", "996609", "996615"], "spl_set_id": ["24290655-47f3-4042-a977-a832c5161d2c"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68180-248-06)", "package_ndc": "68180-248-06", "marketing_start_date": "20180220"}], "brand_name": "memantine hydrochloride", "product_id": "68180-248_2eba035e-38ce-479d-8dc8-0bfdd2bffbcf", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "68180-248", "generic_name": "memantine hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "21 mg/1"}], "application_number": "ANDA206028", "marketing_category": "ANDA", "marketing_start_date": "20180220", "listing_expiration_date": "20271231"}