methylphenidate hydrochloride (72865-123)

Drug Facts

Product Profile

Brand Name methylphenidate hydrochloride

Generic Name methylphenidate hydrochloride

Labeler xlcare pharmaceuticals inc

Dosage Form TABLET

Routes

ORAL

Active Ingredients

methylphenidate hydrochloride 10 mg/1

Manufacturer

XLCare Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 72865-123

Product ID 72865-123_0a38c200-2e90-42b8-97e8-e5b64a7078e0

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA207416

DEA Schedule cii

Listing Expiration 2026-12-31

Marketing Start 2020-02-26

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 72865123

Hyphenated Format 72865-123

Supplemental Identifiers

RxCUI

1091150 1091392 1091497

UPC

0372865124017 0372865123010 0372865122013

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 (source: ndc)

Generic Name methylphenidate hydrochloride (source: ndc)

Application Number ANDA207416 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

10 mg/1

source: ndc

Packaging

100 TABLET in 1 BOTTLE (72865-123-01)
500 TABLET in 1 BOTTLE (72865-123-05)

source: ndc

Packages (2)

72865-123-01 100 TABLET in 1 BOTTLE (72865-123-01) 72865-123-05 500 TABLET in 1 BOTTLE (72865-123-05)

Ingredients (1)

methylphenidate hydrochloride (10 mg/1)

Linked Drug Pages (1)

METHYLPHENIDATE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "0a38c200-2e90-42b8-97e8-e5b64a7078e0", "openfda": {"upc": ["0372865124017", "0372865123010", "0372865122013"], "unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["94dc74d4-b4ef-45bc-b502-54ec692e9bd5"], "manufacturer_name": ["XLCare Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-123-01)", "package_ndc": "72865-123-01", "marketing_start_date": "20200226"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-123-05)", "package_ndc": "72865-123-05", "marketing_start_date": "20200226"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "72865-123_0a38c200-2e90-42b8-97e8-e5b64a7078e0", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72865-123", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "XLCare Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207416", "marketing_category": "ANDA", "marketing_start_date": "20200226", "listing_expiration_date": "20261231"}