Package 55466-122-12

Brand: dexmethylphenidate hydrochloride

Generic: dexmethylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55466-122-12
Digits Only 5546612212
Product NDC 55466-122
Product ID 55466-122_291310a0-43a4-a3a5-e063-6294a90ab7e8
Description

100 TABLET in 1 BOTTLE (55466-122-12)

Marketing

Marketing Status
Marketed Since 2024-03-29
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": "291310a0-43a4-a3a5-e063-6294a90ab7e8", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899518", "899548"], "spl_set_id": ["76b7fd4a-c523-4b35-e053-2a91aa0a4a89"], "manufacturer_name": ["Neolpharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55466-122-12)", "package_ndc": "55466-122-12", "marketing_start_date": "20240329"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "55466-122_291310a0-43a4-a3a5-e063-6294a90ab7e8", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "55466-122", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "Neolpharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209211", "marketing_category": "ANDA", "marketing_start_date": "20240329", "listing_expiration_date": "20261231"}