lisdexamfetamine dimesylate
Generic: lisdexamfetamine dimesylate
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
lisdexamfetamine dimesylate
Generic Name
lisdexamfetamine dimesylate
Labeler
sun pharmaceutical industries, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
lisdexamfetamine dimesylate 70 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
57664-052
Product ID
57664-052_0b77417a-5789-8818-e063-6294a90ad2e3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214484
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2023-08-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
57664052
Hyphenated Format
57664-052
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lisdexamfetamine dimesylate (source: ndc)
Generic Name
lisdexamfetamine dimesylate (source: ndc)
Application Number
ANDA214484 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (57664-052-88)
Packages (1)
Ingredients (1)
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 (57664-052-88)", "package_ndc": "57664-052-88", "marketing_start_date": "20230825"}], "brand_name": "LISDEXAMFETAMINE DIMESYLATE", "product_id": "57664-052_0b77417a-5789-8818-e063-6294a90ad2e3", "dosage_form": "CAPSULE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "57664-052", "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": "70 mg/1"}], "application_number": "ANDA214484", "marketing_category": "ANDA", "marketing_start_date": "20230825", "listing_expiration_date": "20261231"}