dexmethylphenidate hydrochloride extended-release
Generic: dexmethylphenidate hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
dexmethylphenidate hydrochloride extended-release
Generic Name
dexmethylphenidate hydrochloride
Labeler
bryant ranch prepack
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
dexmethylphenidate hydrochloride 15 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621502
Hyphenated Format
72162-1502
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 15 mg/1
Packaging
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1502-1)
Packages (1)
Ingredients (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"}