dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
Generic: dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
Generic Name
dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
amphetamine aspartate monohydrate 1.875 mg/1, amphetamine sulfate 1.875 mg/1, dextroamphetamine saccharate 1.875 mg/1, dextroamphetamine sulfate 1.875 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2049
Product ID
72162-2049_7c8cfbf6-d2da-42dc-92e1-e7792bc591a9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA211352
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2022-12-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622049
Hyphenated Format
72162-2049
Supplemental Identifiers
RxCUI
UNII
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
dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate (source: ndc)
Generic Name
dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate (source: ndc)
Application Number
ANDA211352 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.875 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (72162-2049-1)
- 30 TABLET in 1 BOTTLE (72162-2049-3)
- 60 TABLET in 1 BOTTLE (72162-2049-6)
- 90 TABLET in 1 BOTTLE (72162-2049-9)
Packages (4)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7c8cfbf6-d2da-42dc-92e1-e7792bc591a9", "openfda": {"unii": ["O1ZPV620O4", "6DPV8NK46S", "G83415V073", "JJ768O327N"], "rxcui": ["1009145"], "spl_set_id": ["095f7c39-2685-483a-9d90-47a1398b9dc9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2049-1)", "package_ndc": "72162-2049-1", "marketing_start_date": "20230614"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2049-3)", "package_ndc": "72162-2049-3", "marketing_start_date": "20230614"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-2049-6)", "package_ndc": "72162-2049-6", "marketing_start_date": "20230614"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2049-9)", "package_ndc": "72162-2049-9", "marketing_start_date": "20230614"}], "brand_name": "Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate", "product_id": "72162-2049_7c8cfbf6-d2da-42dc-92e1-e7792bc591a9", "dosage_form": "TABLET", "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": "72162-2049", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate", "active_ingredients": [{"name": "AMPHETAMINE ASPARTATE MONOHYDRATE", "strength": "1.875 mg/1"}, {"name": "AMPHETAMINE SULFATE", "strength": "1.875 mg/1"}, {"name": "DEXTROAMPHETAMINE SACCHARATE", "strength": "1.875 mg/1"}, {"name": "DEXTROAMPHETAMINE SULFATE", "strength": "1.875 mg/1"}], "application_number": "ANDA211352", "marketing_category": "ANDA", "marketing_start_date": "20221229", "listing_expiration_date": "20261231"}