adderall xr
Generic: dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine sulfate and amphetamine aspartate
Labeler: takeda pharmaceuticals america, inc.Drug Facts
Product Profile
Brand Name
adderall xr
Generic Name
dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine sulfate and amphetamine aspartate
Labeler
takeda pharmaceuticals america, inc.
Dosage Form
CAPSULE, EXTENDED RELEASE
Routes
Active Ingredients
amphetamine aspartate monohydrate 6.25 mg/1, amphetamine sulfate 6.25 mg/1, dextroamphetamine saccharate 6.25 mg/1, dextroamphetamine sulfate 6.25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
54092-389
Product ID
54092-389_36ca0eef-16f8-46d7-b92b-1aac1f78d70c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021303
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2002-05-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
54092389
Hyphenated Format
54092-389
Supplemental Identifiers
RxCUI
UPC
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
adderall xr (source: ndc)
Generic Name
dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine sulfate and amphetamine aspartate (source: ndc)
Application Number
NDA021303 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6.25 mg/1
Packaging
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54092-389-01)
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36ca0eef-16f8-46d7-b92b-1aac1f78d70c", "openfda": {"upc": ["0354092387014", "0354092391011"], "unii": ["O1ZPV620O4", "6DPV8NK46S", "G83415V073", "JJ768O327N"], "rxcui": ["861221", "861222", "861223", "861224", "861225", "861226", "861227", "861228", "861232", "861233", "861237", "861238"], "spl_set_id": ["aff45863-ffe1-4d4f-8acf-c7081512a6c0"], "manufacturer_name": ["Takeda Pharmaceuticals America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54092-389-01)", "package_ndc": "54092-389-01", "marketing_start_date": "20020522"}], "brand_name": "Adderall XR", "product_id": "54092-389_36ca0eef-16f8-46d7-b92b-1aac1f78d70c", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]", "Central Nervous System Stimulation [PE]", "Central Nervous System Stimulation [PE]", "Central Nervous System Stimulation [PE]"], "product_ndc": "54092-389", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Sulfate, Dextroamphetamine Saccharate, Amphetamine Sulfate and Amphetamine Aspartate", "labeler_name": "Takeda Pharmaceuticals America, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Adderall", "brand_name_suffix": "XR", "active_ingredients": [{"name": "AMPHETAMINE ASPARTATE MONOHYDRATE", "strength": "6.25 mg/1"}, {"name": "AMPHETAMINE SULFATE", "strength": "6.25 mg/1"}, {"name": "DEXTROAMPHETAMINE SACCHARATE", "strength": "6.25 mg/1"}, {"name": "DEXTROAMPHETAMINE SULFATE", "strength": "6.25 mg/1"}], "application_number": "NDA021303", "marketing_category": "NDA", "marketing_start_date": "20020522", "listing_expiration_date": "20261231"}