Package 10702-076-06

{"route": ["ORAL"], "spl_id": "40950048-0e42-4661-e063-6394a90a2bb1", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091145", "1091225"], "spl_set_id": ["be8580bc-0eb2-4eb6-a4cc-4ebbeb33424d"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-076-01)", "package_ndc": "10702-076-01", "marketing_start_date": "20150609"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (10702-076-06)", "package_ndc": "10702-076-06", "marketing_start_date": "20150609"}], "brand_name": "METHYLPHENIDATE HYDROCHLORIDE EXTENDED RELEASE", "product_id": "10702-076_40950048-0e42-4661-e063-6394a90a2bb1", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "10702-076", "dea_schedule": "CII", "generic_name": "methylphenidate hydrochloride extended release", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPHENIDATE HYDROCHLORIDE EXTENDED RELEASE", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA207488", "marketing_category": "ANDA", "marketing_start_date": "20150609", "listing_expiration_date": "20261231"}