methylphenidate hydrochloride cd

Generic: methylphenidate hydrochloride

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name methylphenidate hydrochloride cd
Generic Name methylphenidate hydrochloride
Labeler lannett company, inc.
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

methylphenidate hydrochloride 30 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-4581
Product ID 0527-4581_bd13224e-942e-4866-88b9-8729c89204e7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021259
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2003-07-22

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 05274581
Hyphenated Format 0527-4581

Supplemental Identifiers

RxCUI
1806181 1806187 1806189 1806191 1806193 1806197
UPC
0305274579376 0305274580372 0305274584370
UNII
4B3SC438HI

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 methylphenidate hydrochloride cd (source: ndc)
Generic Name methylphenidate hydrochloride (source: ndc)
Application Number NDA021259 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4581-37)
source: ndc

Packages (1)

0527-4581-37 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4581-37)

Ingredients (1)

methylphenidate hydrochloride (30 mg/1)

Linked Drug Pages (1)

methylphenidate hydrochloride CD ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bd13224e-942e-4866-88b9-8729c89204e7", "openfda": {"upc": ["0305274579376", "0305274580372", "0305274584370"], "unii": ["4B3SC438HI"], "rxcui": ["1806181", "1806187", "1806189", "1806191", "1806193", "1806197"], "spl_set_id": ["e45c75dc-d381-475b-b649-a871c8a36e60"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0527-4581-37)", "package_ndc": "0527-4581-37", "marketing_start_date": "20030722"}], "brand_name": "methylphenidate hydrochloride CD", "product_id": "0527-4581_bd13224e-942e-4866-88b9-8729c89204e7", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0527-4581", "dea_schedule": "CII", "generic_name": "methylphenidate hydrochloride", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "methylphenidate hydrochloride CD", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA021259", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20030722", "listing_expiration_date": "20261231"}