Package 27808-092-01

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 27808-092-01
Digits Only 2780809201
Product NDC 27808-092
Product ID 27808-092_9e21f04a-b4b6-45b8-8da3-5955e6aa18a5
Description

100 TABLET in 1 BOTTLE (27808-092-01)

Marketing

Marketing Status
Marketed Since 2001-11-30
Brand dexmethylphenidate hydrochloride
Generic dexmethylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Dexmethylphenidate Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9e21f04a-b4b6-45b8-8da3-5955e6aa18a5", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899518", "899548", "899557"], "spl_set_id": ["1f2aa66a-51dc-459c-a765-5364bccd310f"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (27808-092-01)", "package_ndc": "27808-092-01", "marketing_start_date": "20011130"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "27808-092_9e21f04a-b4b6-45b8-8da3-5955e6aa18a5", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "27808-092", "dea_schedule": "CII", "generic_name": "dexmethylphenidate hydrochloride", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA207901", "marketing_category": "ANDA", "marketing_start_date": "20011130", "listing_expiration_date": "20261231"}