dexmethylphenidate hydrochloride
Generic: dexmethylphenidate hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
dexmethylphenidate hydrochloride
Generic Name
dexmethylphenidate hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
dexmethylphenidate hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63629-2307
Product ID
63629-2307_e3e20e09-b76f-487f-802e-dd26ccdd753d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207901
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2001-11-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636292307
Hyphenated Format
63629-2307
Supplemental Identifiers
RxCUI
UNII
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
dexmethylphenidate hydrochloride (source: ndc)
Generic Name
dexmethylphenidate hydrochloride (source: ndc)
Application Number
ANDA207901 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE, PLASTIC (63629-2307-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e3e20e09-b76f-487f-802e-dd26ccdd753d", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899548"], "spl_set_id": ["f88da72d-c22f-413b-9dce-60871299b06a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (63629-2307-1)", "package_ndc": "63629-2307-1", "marketing_start_date": "20211222"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "63629-2307_e3e20e09-b76f-487f-802e-dd26ccdd753d", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "63629-2307", "dea_schedule": "CII", "generic_name": "dexmethylphenidate hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207901", "marketing_category": "ANDA", "marketing_start_date": "20011130", "listing_expiration_date": "20261231"}