Package 49884-546-01
Brand: dexmethylphenidate hydrochloride
Generic: dexmethylphenidate hydrochloridePackage Facts
Identity
Package NDC
49884-546-01
Digits Only
4988454601
Product NDC
49884-546
Description
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-546-01)
Marketing
Marketing Status
Brand
dexmethylphenidate hydrochloride
Generic
dexmethylphenidate hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "09fcee97-8b48-4a1d-a380-0e01c92e0e9b", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899439", "899461", "899485", "899495", "899511", "1006608", "1101926", "1101932"], "spl_set_id": ["e304388e-86a6-4335-abae-0ce79c7c99c6"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (49884-546-01)", "package_ndc": "49884-546-01", "marketing_start_date": "20170105"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "49884-546_09fcee97-8b48-4a1d-a380-0e01c92e0e9b", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "49884-546", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA202842", "marketing_category": "ANDA", "marketing_start_date": "20170105", "listing_expiration_date": "20261231"}