methylphenidate hydrochloride

Generic: methylphenidate hydrochloride

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

Drug Facts

Product Profile

Brand Name methylphenidate hydrochloride
Generic Name methylphenidate hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methylphenidate hydrochloride 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2019
Product ID 72162-2019_13a17c5a-bba7-4c5a-a4f9-2141bcdffa1a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091159
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2014-04-07

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 721622019
Hyphenated Format 72162-2019

Supplemental Identifiers

RxCUI
1091497
UNII
4B3SC438HI

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 ANDA091159 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72162-2019-1)
  • 60 TABLET in 1 BOTTLE (72162-2019-6)
source: ndc

Packages (2)

72162-2019-1 100 TABLET in 1 BOTTLE (72162-2019-1) 72162-2019-6 60 TABLET in 1 BOTTLE (72162-2019-6)

Ingredients (1)

methylphenidate hydrochloride (5 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": "13a17c5a-bba7-4c5a-a4f9-2141bcdffa1a", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091497"], "spl_set_id": ["13a17c5a-bba7-4c5a-a4f9-2141bcdffa1a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2019-1)", "package_ndc": "72162-2019-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-2019-6)", "package_ndc": "72162-2019-6", "marketing_start_date": "20240403"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "72162-2019_13a17c5a-bba7-4c5a-a4f9-2141bcdffa1a", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2019", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091159", "marketing_category": "ANDA", "marketing_start_date": "20140407", "listing_expiration_date": "20261231"}