dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride

Labeler: kvk-tech, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexmethylphenidate hydrochloride
Generic Name dexmethylphenidate hydrochloride
Labeler kvk-tech, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dexmethylphenidate hydrochloride 2.5 mg/1

Manufacturer
KVK-TECH, INC

Identifiers & Regulatory

Product NDC 10702-106
Product ID 10702-106_445dff50-b3a4-8602-e063-6294a90aef3b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206931
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-12-04

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 10702106
Hyphenated Format 10702-106

Supplemental Identifiers

RxCUI
899518 899548 899557
UPC
0310702108011 0310702106017 0310702107014
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 dexmethylphenidate hydrochloride (source: ndc)
Generic Name dexmethylphenidate hydrochloride (source: ndc)
Application Number ANDA206931 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (10702-106-01)
source: ndc

Packages (1)

10702-106-01 100 TABLET in 1 BOTTLE (10702-106-01)

Ingredients (1)

dexmethylphenidate hydrochloride (2.5 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": "445dff50-b3a4-8602-e063-6294a90aef3b", "openfda": {"upc": ["0310702108011", "0310702106017", "0310702107014"], "unii": ["1678OK0E08"], "rxcui": ["899518", "899548", "899557"], "spl_set_id": ["0c717ae4-ec27-47db-ac1b-e504dbb379be"], "manufacturer_name": ["KVK-TECH, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-106-01)", "package_ndc": "10702-106-01", "marketing_start_date": "20151204"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "10702-106_445dff50-b3a4-8602-e063-6294a90aef3b", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "10702-106", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "KVK-TECH, INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA206931", "marketing_category": "ANDA", "marketing_start_date": "20151204", "listing_expiration_date": "20261231"}