Package 0093-5347-01
Brand: methylphenidate hydrochloride (la)
Generic: methylphenidate hydrochloridePackage Facts
Identity
Package NDC
0093-5347-01
Digits Only
0093534701
Product NDC
0093-5347
Description
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5347-01)
Marketing
Marketing Status
Brand
methylphenidate hydrochloride (la)
Generic
methylphenidate hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "663ba889-95b5-45c2-af06-c90459d30d6d", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1806177", "1806179", "1806183"], "spl_set_id": ["034fb7cd-e183-475e-8beb-64fd88facc8f"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-5347-01)", "package_ndc": "0093-5347-01", "marketing_start_date": "20120716"}], "brand_name": "Methylphenidate Hydrochloride (LA)", "product_id": "0093-5347_663ba889-95b5-45c2-af06-c90459d30d6d", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0093-5347", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "brand_name_suffix": "(LA)", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA079031", "marketing_category": "ANDA", "marketing_start_date": "20120716", "listing_expiration_date": "20261231"}