Package 60760-779-30

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-779-30
Digits Only 6076077930
Product NDC 60760-779
Product ID 60760-779_3dd7e808-e0ec-8514-e063-6394a90a9f34
Description

30 CAPSULE in 1 BOTTLE, PLASTIC (60760-779-30)

Marketing

Marketing Status
Marketed Since 2025-08-26
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": "3dd7e808-e0ec-8514-e063-6394a90a9f34", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["3dd7f2a6-5a91-81a2-e063-6294a90a33db"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (60760-779-30)", "package_ndc": "60760-779-30", "marketing_start_date": "20250826"}], "brand_name": "Amantadine Hydrochloride", "product_id": "60760-779_3dd7e808-e0ec-8514-e063-6394a90a9f34", "dosage_form": "CAPSULE", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "60760-779", "generic_name": "Amantadine Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine Hydrochloride", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA212044", "marketing_category": "ANDA", "marketing_start_date": "20200521", "listing_expiration_date": "20261231"}