Package 71335-2919-1

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2919-1
Digits Only 7133529191
Product NDC 71335-2919
Product ID 71335-2919_baf21fd8-402e-47b4-8b1a-d0ffca88dd3b
Description

500 CAPSULE in 1 BOTTLE (71335-2919-1)

Marketing

Marketing Status
Marketed Since 2025-10-22
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": "baf21fd8-402e-47b4-8b1a-d0ffca88dd3b", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["a10bf8b5-bf70-4090-b4b2-a0be252b9fe4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 CAPSULE in 1 BOTTLE (71335-2919-1)", "package_ndc": "71335-2919-1", "marketing_start_date": "20251022"}], "brand_name": "Amantadine Hydrochloride", "product_id": "71335-2919_baf21fd8-402e-47b4-8b1a-d0ffca88dd3b", "dosage_form": "CAPSULE", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "71335-2919", "generic_name": "Amantadine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine Hydrochloride", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA209171", "marketing_category": "ANDA", "marketing_start_date": "20170612", "listing_expiration_date": "20261231"}