methylphenidate hydrochloride
Generic: methylphenidate hydrochloride
Labeler: cranbury pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
methylphenidate hydrochloride
Generic Name
methylphenidate hydrochloride
Labeler
cranbury pharmaceuticals, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
methylphenidate hydrochloride 5 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
27808-058
Product ID
27808-058_2b5b76ed-a330-4f7b-a111-467a067ee663
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091601
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2015-03-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
27808058
Hyphenated Format
27808-058
Supplemental Identifiers
RxCUI
UPC
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
ANDA091601 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/5mL
Packaging
- 500 mL in 1 BOTTLE, PLASTIC (27808-058-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b5b76ed-a330-4f7b-a111-467a067ee663", "openfda": {"upc": ["0327808059017"], "unii": ["4B3SC438HI"], "rxcui": ["1091133", "1091341"], "spl_set_id": ["e817377f-bc72-415a-acd2-7136746b2479"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (27808-058-01)", "package_ndc": "27808-058-01", "marketing_start_date": "20150304"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "27808-058_2b5b76ed-a330-4f7b-a111-467a067ee663", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "27808-058", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/5mL"}], "application_number": "ANDA091601", "marketing_category": "ANDA", "marketing_start_date": "20150304", "listing_expiration_date": "20261231"}