Package 60687-565-21
Brand: methylphenidate hydrochloride
Generic: methylphenidate hydrochloridePackage Facts
Identity
Package NDC
60687-565-21
Digits Only
6068756521
Product NDC
60687-565
Description
30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-565-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-565-11)
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": "4522b794-5c43-44cd-e063-6394a90ab39a", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091155", "1091170", "1091185", "1091210"], "spl_set_id": ["f6581305-cd1e-4171-8c1b-e184c7bde033"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-565-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-565-11)", "package_ndc": "60687-565-21", "marketing_start_date": "20240922"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "60687-565_4522b794-5c43-44cd-e063-6394a90ab39a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "60687-565", "dea_schedule": "CII", "generic_name": "Methylphenidate Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "54 mg/1"}], "application_number": "ANDA211009", "marketing_category": "ANDA", "marketing_start_date": "20200625", "listing_expiration_date": "20261231"}