Package 31722-173-01
Brand: methylphenidate hydrochloride
Generic: methylphenidate hydrochloridePackage Facts
Identity
Package NDC
31722-173-01
Digits Only
3172217301
Product NDC
31722-173
Description
100 TABLET in 1 BOTTLE (31722-173-01)
Marketing
Marketing Status
Brand
methylphenidate hydrochloride
Generic
methylphenidate hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "85610552-360d-4ae3-b160-0819534f8220", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091392", "1091497"], "spl_set_id": ["778190da-1528-4def-94bf-ee23ee5268a5"], "manufacturer_name": ["Camber Pharmaceutical Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-173-01)", "package_ndc": "31722-173-01", "marketing_start_date": "20151001"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-173-05)", "package_ndc": "31722-173-05", "marketing_start_date": "20151001"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE", "product_id": "31722-173_85610552-360d-4ae3-b160-0819534f8220", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "31722-173", "dea_schedule": "CII", "generic_name": "METHYLPHENIDATE HYDROCHLORIDE", "labeler_name": "Camber Pharmaceutical Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA207416", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}