amantadine hydrochloride
Generic: amantadine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
amantadine hydrochloride
Generic Name
amantadine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
CAPSULE
Routes
Active Ingredients
amantadine hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-2959
Product ID
71335-2959_99e43d39-01e6-445c-a222-78b4fb8b5cd3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209171
Listing Expiration
2026-12-31
Marketing Start
2017-06-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352959
Hyphenated Format
71335-2959
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
amantadine hydrochloride (source: ndc)
Generic Name
amantadine hydrochloride (source: ndc)
Application Number
ANDA209171 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (71335-2959-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "99e43d39-01e6-445c-a222-78b4fb8b5cd3", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["96aefbca-fe71-42ef-8079-d0d9e7370ccb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-2959-1)", "package_ndc": "71335-2959-1", "marketing_start_date": "20251022"}], "brand_name": "Amantadine Hydrochloride", "product_id": "71335-2959_99e43d39-01e6-445c-a222-78b4fb8b5cd3", "dosage_form": "CAPSULE", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "71335-2959", "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"}