Package 67046-1452-3

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1452-3
Digits Only 6704614523
Product NDC 67046-1452
Description

30 TABLET in 1 BLISTER PACK (67046-1452-3)

Marketing

Marketing Status
Marketed Since 2025-02-07
Brand amantadine hydrochloride
Generic amantadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d940d35-6a65-e494-e063-6394a90a9d16", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849395"], "spl_set_id": ["2d94073b-c064-c280-e063-6294a90af145"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1452-3)", "package_ndc": "67046-1452-3", "marketing_start_date": "20250207"}], "brand_name": "Amantadine Hydrochloride", "product_id": "67046-1452_2d940d35-6a65-e494-e063-6394a90a9d16", "dosage_form": "TABLET", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "67046-1452", "generic_name": "Amantadine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine Hydrochloride", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA209035", "marketing_category": "ANDA", "marketing_start_date": "20250207", "listing_expiration_date": "20261231"}