amantadine hydrochloride

Generic: amantadine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amantadine hydrochloride
Generic Name amantadine hydrochloride
Labeler bryant ranch prepack
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

amantadine hydrochloride 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0469
Product ID 71335-0469_3ef002b2-c3df-4474-92d6-940444cc9415
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208278
Listing Expiration 2026-12-31
Marketing Start 2016-08-04

Pharmacologic Class

Classes
influenza a m2 protein inhibitor [epc] m2 protein inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350469
Hyphenated Format 71335-0469

Supplemental Identifiers

RxCUI
849389
UNII
M6Q1EO9TD0

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 ANDA208278 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 20 CAPSULE in 1 BOTTLE (71335-0469-1)
  • 30 CAPSULE in 1 BOTTLE (71335-0469-2)
  • 10 CAPSULE in 1 BOTTLE (71335-0469-3)
  • 14 CAPSULE in 1 BOTTLE (71335-0469-4)
  • 60 CAPSULE in 1 BOTTLE (71335-0469-5)
  • 100 CAPSULE in 1 BOTTLE (71335-0469-6)
source: ndc

Packages (6)

71335-0469-1 20 CAPSULE in 1 BOTTLE (71335-0469-1) 71335-0469-2 30 CAPSULE in 1 BOTTLE (71335-0469-2) 71335-0469-3 10 CAPSULE in 1 BOTTLE (71335-0469-3) 71335-0469-4 14 CAPSULE in 1 BOTTLE (71335-0469-4) 71335-0469-5 60 CAPSULE in 1 BOTTLE (71335-0469-5) 71335-0469-6 100 CAPSULE in 1 BOTTLE (71335-0469-6)

Ingredients (1)

amantadine hydrochloride (100 mg/1)

Linked Drug Pages (1)

amantadine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ef002b2-c3df-4474-92d6-940444cc9415", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["8e578f11-6112-4a1f-8de4-a76870bb62c7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 CAPSULE in 1 BOTTLE (71335-0469-1)", "package_ndc": "71335-0469-1", "marketing_start_date": "20211227"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-0469-2)", "package_ndc": "71335-0469-2", "marketing_start_date": "20210830"}, {"sample": false, "description": "10 CAPSULE in 1 BOTTLE (71335-0469-3)", "package_ndc": "71335-0469-3", "marketing_start_date": "20211227"}, {"sample": false, "description": "14 CAPSULE in 1 BOTTLE (71335-0469-4)", "package_ndc": "71335-0469-4", "marketing_start_date": "20181022"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-0469-5)", "package_ndc": "71335-0469-5", "marketing_start_date": "20200805"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-0469-6)", "package_ndc": "71335-0469-6", "marketing_start_date": "20200805"}], "brand_name": "amantadine hydrochloride", "product_id": "71335-0469_3ef002b2-c3df-4474-92d6-940444cc9415", "dosage_form": "CAPSULE", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "71335-0469", "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": "ANDA208278", "marketing_category": "ANDA", "marketing_start_date": "20160804", "listing_expiration_date": "20261231"}