Package 31722-232-01

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-232-01
Digits Only 3172223201
Product NDC 31722-232
Product ID 31722-232_81c8ba81-82ac-4c18-b28b-da9c71520f35
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-232-01)

Marketing

Marketing Status
Marketed Since 2021-12-08
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": "81c8ba81-82ac-4c18-b28b-da9c71520f35", "openfda": {"upc": ["0331722233019", "0331722229012", "0331722234016", "0331722235013", "0331722231015", "0331722236010", "0331722232012", "0331722230018"], "unii": ["1678OK0E08"], "rxcui": ["899439", "899461", "899485", "899495", "899511", "1006608", "1101926", "1101932"], "spl_set_id": ["77659abe-74be-4092-90fe-cc475726d4ec"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-232-01)", "package_ndc": "31722-232-01", "marketing_start_date": "20211208"}], "brand_name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "product_id": "31722-232_81c8ba81-82ac-4c18-b28b-da9c71520f35", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "31722-232", "dea_schedule": "CII", "generic_name": "dexmethylphenidate hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA215523", "marketing_category": "ANDA", "marketing_start_date": "20211208", "listing_expiration_date": "20261231"}