Package 57664-049-88
Brand: lisdexamfetamine dimesylate
Generic: lisdexamfetamine dimesylatePackage Facts
Identity
Package NDC
57664-049-88
Digits Only
5766404988
Product NDC
57664-049
Description
100 CAPSULE in 1 BOTTLE (57664-049-88)
Marketing
Marketing Status
Brand
lisdexamfetamine dimesylate
Generic
lisdexamfetamine dimesylate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0b77417a-5789-8818-e063-6294a90ad2e3", "openfda": {"unii": ["SJT761GEGS"], "rxcui": ["854830", "854834", "854838", "854842", "854846", "854850", "1593856", "1871456", "1871460", "1871462", "1871464", "1871466", "1871468"], "spl_set_id": ["da3148af-f9b6-4725-adae-3595b4c7dc4b"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (57664-049-88)", "package_ndc": "57664-049-88", "marketing_start_date": "20230825"}], "brand_name": "LISDEXAMFETAMINE DIMESYLATE", "product_id": "57664-049_0b77417a-5789-8818-e063-6294a90ad2e3", "dosage_form": "CAPSULE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "57664-049", "dea_schedule": "CII", "generic_name": "LISDEXAMFETAMINE DIMESYLATE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISDEXAMFETAMINE DIMESYLATE", "active_ingredients": [{"name": "LISDEXAMFETAMINE DIMESYLATE", "strength": "40 mg/1"}], "application_number": "ANDA214484", "marketing_category": "ANDA", "marketing_start_date": "20230825", "listing_expiration_date": "20261231"}