amantadine
Generic: amantadine
Labeler: alembic pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
amantadine
Generic Name
amantadine
Labeler
alembic pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
amantadine hydrochloride 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62332-586
Product ID
62332-586_a9507ffa-0c95-48ce-80bf-60bc699add17
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214284
Listing Expiration
2026-12-31
Marketing Start
2020-10-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62332586
Hyphenated Format
62332-586
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 (source: ndc)
Generic Name
amantadine (source: ndc)
Application Number
ANDA214284 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (62332-586-31)
- 500 TABLET in 1 BOTTLE (62332-586-71)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a9507ffa-0c95-48ce-80bf-60bc699add17", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849395"], "spl_set_id": ["da1837b5-fda2-48e0-91ba-d6eb2b991b55"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62332-586-31)", "package_ndc": "62332-586-31", "marketing_start_date": "20201020"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (62332-586-71)", "package_ndc": "62332-586-71", "marketing_start_date": "20201020"}], "brand_name": "Amantadine", "product_id": "62332-586_a9507ffa-0c95-48ce-80bf-60bc699add17", "dosage_form": "TABLET", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "62332-586", "generic_name": "Amantadine", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA214284", "marketing_category": "ANDA", "marketing_start_date": "20201020", "listing_expiration_date": "20261231"}