Package 68084-805-21

Brand: methylphenidate hydrochloride

Generic: methylphenidate hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68084-805-21
Digits Only 6808480521
Product NDC 68084-805
Product ID 68084-805_41c22d0f-0fbe-e5af-e063-6294a90a47c0
Description

30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-805-21) / 1 TABLET in 1 BLISTER PACK (68084-805-11)

Marketing

Marketing Status
Marketed Since 2014-09-30
Brand methylphenidate hydrochloride
Generic methylphenidate hydrochloride
Sample Package No

Linked Drug Pages (1)

Methylphenidate Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41c22d0f-0fbe-e5af-e063-6294a90a47c0", "openfda": {"unii": ["4B3SC438HI"], "rxcui": ["1091150", "1091497"], "spl_set_id": ["eb9b7377-d918-43fb-8e82-d14c85ed64a8"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-805-21)  / 1 TABLET in 1 BLISTER PACK (68084-805-11)", "package_ndc": "68084-805-21", "marketing_start_date": "20140930"}], "brand_name": "Methylphenidate Hydrochloride", "product_id": "68084-805_41c22d0f-0fbe-e5af-e063-6294a90a47c0", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "68084-805", "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": "5 mg/1"}], "application_number": "ANDA040300", "marketing_category": "ANDA", "marketing_start_date": "20140930", "listing_expiration_date": "20261231"}