methylphenidate hydrochloride
Generic: methylphenidate hydrochloride
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
methylphenidate hydrochloride
Generic Name
methylphenidate hydrochloride
Labeler
rising pharma holdings, inc.
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
methylphenidate hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
64980-222
Product ID
64980-222_85d614b0-888e-461f-bc7d-3f240ed8bd0e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205756
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2018-12-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64980222
Hyphenated Format
64980-222
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA205756 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 TABLET, CHEWABLE in 1 BOTTLE (64980-222-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "85d614b0-888e-461f-bc7d-3f240ed8bd0e", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091152", "1091322", "1091389"], "spl_set_id": ["e5cb0740-813f-4dce-8c29-d7680c66e77c"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, CHEWABLE in 1 BOTTLE (64980-222-01)", "package_ndc": "64980-222-01", "marketing_start_date": "20181218"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "64980-222_85d614b0-888e-461f-bc7d-3f240ed8bd0e", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "64980-222", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA205756", "marketing_category": "ANDA", "marketing_start_date": "20181218", "listing_expiration_date": "20261231"}