dextroamphetamine sulfate
Generic: dextroamphetamine sulfate
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
dextroamphetamine sulfate
Generic Name
dextroamphetamine sulfate
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
dextroamphetamine sulfate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72162-2350
Product ID
72162-2350_9dd752c2-6687-4190-a3b5-ca2c1c6a0ba4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090533
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2012-07-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721622350
Hyphenated Format
72162-2350
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 sulfate (source: ndc)
Generic Name
dextroamphetamine sulfate (source: ndc)
Application Number
ANDA090533 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (72162-2350-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9dd752c2-6687-4190-a3b5-ca2c1c6a0ba4", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884385"], "spl_set_id": ["54b122b0-2ec8-43c9-86e8-a3538a83c776"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2350-3)", "package_ndc": "72162-2350-3", "marketing_start_date": "20210414"}], "brand_name": "Dextroamphetamine Sulfate", "product_id": "72162-2350_9dd752c2-6687-4190-a3b5-ca2c1c6a0ba4", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2350", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Sulfate", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA090533", "marketing_category": "ANDA", "marketing_start_date": "20120720", "listing_expiration_date": "20261231"}