Package 61037-484-03

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 61037-484-03
Digits Only 6103748403
Product NDC 61037-484
Product ID 61037-484_38fc829b-496d-024d-e063-6294a90a11b5
Description

473 mL in 1 BOTTLE (61037-484-03)

Marketing

Marketing Status
Marketed Since 2025-07-31
Brand amantadine hydrochloride
Generic amantadine hydrochloride
Sample Package No

Linked Drug Pages (1)

AMANTADINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38fc829b-496d-024d-e063-6294a90a11b5", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849385"], "spl_set_id": ["38fccce5-1f1e-9350-e063-6394a90a045a"], "manufacturer_name": ["BAJAJ MEDICAL, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (61037-484-03)", "package_ndc": "61037-484-03", "marketing_start_date": "20250731"}], "brand_name": "AMANTADINE HYDROCHLORIDE", "product_id": "61037-484_38fc829b-496d-024d-e063-6294a90a11b5", "dosage_form": "SOLUTION", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "61037-484", "generic_name": "AMANTADINE HYDROCHLORIDE", "labeler_name": "BAJAJ MEDICAL, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMANTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "50 mg/5mL"}], "application_number": "ANDA075819", "marketing_category": "ANDA", "marketing_start_date": "20250731", "listing_expiration_date": "20261231"}