dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride

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

Drug Facts

Product Profile

Brand Name dexmethylphenidate hydrochloride
Generic Name dexmethylphenidate hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dexmethylphenidate hydrochloride 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2426
Product ID 72162-2426_855db90f-4912-49f3-bf34-0548bf3df04e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209211
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2024-05-03

Pharmacologic Class

Classes
central nervous system stimulant [epc] central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622426
Hyphenated Format 72162-2426

Supplemental Identifiers

RxCUI
899518
UNII
1678OK0E08

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 dexmethylphenidate hydrochloride (source: ndc)
Generic Name dexmethylphenidate hydrochloride (source: ndc)
Application Number ANDA209211 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-2426-1)
  • 60 TABLET in 1 BOTTLE (72162-2426-6)
source: ndc

Packages (2)

72162-2426-1 100 TABLET in 1 BOTTLE (72162-2426-1) 72162-2426-6 60 TABLET in 1 BOTTLE (72162-2426-6)

Ingredients (1)

dexmethylphenidate hydrochloride (5 mg/1)

Linked Drug Pages (1)

Dexmethylphenidate hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "855db90f-4912-49f3-bf34-0548bf3df04e", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899518"], "spl_set_id": ["90308fd0-d174-4979-aa22-16290d6cc5bb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2426-1)", "package_ndc": "72162-2426-1", "marketing_start_date": "20241118"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-2426-6)", "package_ndc": "72162-2426-6", "marketing_start_date": "20241118"}], "brand_name": "Dexmethylphenidate hydrochloride", "product_id": "72162-2426_855db90f-4912-49f3-bf34-0548bf3df04e", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2426", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209211", "marketing_category": "ANDA", "marketing_start_date": "20240503", "listing_expiration_date": "20261231"}