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 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1219
Product ID 71335-1219_6183e88c-f148-4ee3-a49c-6e7aee7009bc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207416
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-10-01

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 713351219
Hyphenated Format 71335-1219

Supplemental Identifiers

RxCUI
1091392
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 ANDA207416 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1219-1)
  • 100 TABLET in 1 BOTTLE (71335-1219-2)
  • 90 TABLET in 1 BOTTLE (71335-1219-3)
  • 60 TABLET in 1 BOTTLE (71335-1219-4)
  • 120 TABLET in 1 BOTTLE (71335-1219-5)
source: ndc

Packages (5)

71335-1219-1 30 TABLET in 1 BOTTLE (71335-1219-1) 71335-1219-2 100 TABLET in 1 BOTTLE (71335-1219-2) 71335-1219-3 90 TABLET in 1 BOTTLE (71335-1219-3) 71335-1219-4 60 TABLET in 1 BOTTLE (71335-1219-4) 71335-1219-5 120 TABLET in 1 BOTTLE (71335-1219-5)

Ingredients (1)

methylphenidate hydrochloride (20 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": "6183e88c-f148-4ee3-a49c-6e7aee7009bc", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091392"], "spl_set_id": ["ec3d9304-13bc-4f0b-bf14-1a1ea824bd91"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1219-1)", "package_ndc": "71335-1219-1", "marketing_start_date": "20241031"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1219-2)", "package_ndc": "71335-1219-2", "marketing_start_date": "20241031"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1219-3)", "package_ndc": "71335-1219-3", "marketing_start_date": "20190424"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1219-4)", "package_ndc": "71335-1219-4", "marketing_start_date": "20190424"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1219-5)", "package_ndc": "71335-1219-5", "marketing_start_date": "20241031"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "71335-1219_6183e88c-f148-4ee3-a49c-6e7aee7009bc", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "71335-1219", "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": "20 mg/1"}], "application_number": "ANDA207416", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}