ritalin

Generic: methylphenidate hydrochloride

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ritalin
Generic Name methylphenidate hydrochloride
Labeler sandoz inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methylphenidate hydrochloride 5 mg/1

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 66758-273
Product ID 66758-273_3cf2c541-a65c-4651-ab30-3451a5581f8f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA010187
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 1955-12-31

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 66758273
Hyphenated Format 66758-273

Supplemental Identifiers

RxCUI
1091150 1091379 1091392 1091395 1091497 1091500
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 ritalin (source: ndc)
Generic Name methylphenidate hydrochloride (source: ndc)
Application Number NDA010187 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (66758-273-01)
source: ndc

Packages (1)

66758-273-01 100 TABLET in 1 BOTTLE (66758-273-01)

Ingredients (1)

methylphenidate hydrochloride (5 mg/1)

Linked Drug Pages (1)

Ritalin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cf2c541-a65c-4651-ab30-3451a5581f8f", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091379", "1091392", "1091395", "1091497", "1091500"], "spl_set_id": ["d6fb2750-cdab-4749-ba0d-7534840a5892"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66758-273-01)", "package_ndc": "66758-273-01", "marketing_start_date": "20250728"}], "brand_name": "Ritalin", "product_id": "66758-273_3cf2c541-a65c-4651-ab30-3451a5581f8f", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "66758-273", "dea_schedule": "CII", "generic_name": "methylphenidate hydrochloride", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ritalin", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "NDA010187", "marketing_category": "NDA", "marketing_start_date": "19551231", "listing_expiration_date": "20261231"}