dexmethylphenidate hydrochloride extended-release

Generic: dexmethylphenidate hydrochloride

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

Drug Facts

Product Profile

Brand Name dexmethylphenidate hydrochloride extended-release
Generic Name dexmethylphenidate hydrochloride
Labeler bryant ranch prepack
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

dexmethylphenidate hydrochloride 15 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1502
Product ID 72162-1502_51f04bf3-77fc-4f1a-a024-ef3d7ede8955
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078992
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2013-11-19

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 721621502
Hyphenated Format 72162-1502

Supplemental Identifiers

RxCUI
899461
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 extended-release (source: ndc)
Generic Name dexmethylphenidate hydrochloride (source: ndc)
Application Number ANDA078992 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1502-1)
source: ndc

Packages (1)

Ingredients (1)

dexmethylphenidate hydrochloride (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "51f04bf3-77fc-4f1a-a024-ef3d7ede8955", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899461"], "spl_set_id": ["32b3c189-f0f8-4f3e-87da-ce56f583fc42"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1502-1)", "package_ndc": "72162-1502-1", "marketing_start_date": "20131119"}], "brand_name": "Dexmethylphenidate Hydrochloride Extended-Release", "product_id": "72162-1502_51f04bf3-77fc-4f1a-a024-ef3d7ede8955", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1502", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA078992", "marketing_category": "ANDA", "marketing_start_date": "20131119", "listing_expiration_date": "20261231"}