focalin

Generic: dexmethylphenidate hydrochloride

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name focalin
Generic Name dexmethylphenidate hydrochloride
Labeler sandoz inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dexmethylphenidate hydrochloride 2.5 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 66758-250
Product ID 66758-250_b5989bf2-41d3-4bd9-82aa-d89923911cd1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021278
DEA Schedule cii
Marketing Start 2001-11-30
Marketing End 2027-09-30

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 66758250
Hyphenated Format 66758-250

Supplemental Identifiers

RxCUI
899518 899519 899548 899549 899557 899559
UNII
1678OK0E08

Packaging Origin

Original Packager
true

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 focalin (source: ndc)
Generic Name dexmethylphenidate hydrochloride (source: ndc)
Application Number NDA021278 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (66758-250-01)
source: ndc

Packages (1)

66758-250-01 100 TABLET in 1 BOTTLE (66758-250-01)

Ingredients (1)

dexmethylphenidate hydrochloride (2.5 mg/1)

Linked Drug Pages (1)

Focalin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b5989bf2-41d3-4bd9-82aa-d89923911cd1", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899518", "899519", "899548", "899549", "899557", "899559"], "spl_set_id": ["2016f5c2-95d2-4655-af65-c588c2bf5e6d"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66758-250-01)", "package_ndc": "66758-250-01", "marketing_end_date": "20270731", "marketing_start_date": "20240816"}], "brand_name": "Focalin", "product_id": "66758-250_b5989bf2-41d3-4bd9-82aa-d89923911cd1", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "66758-250", "dea_schedule": "CII", "generic_name": "dexmethylphenidate hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Focalin", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "NDA021278", "marketing_category": "NDA", "marketing_end_date": "20270930", "marketing_start_date": "20011130"}