dextroamphetamine

Generic: dextroamphetamine

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextroamphetamine
Generic Name dextroamphetamine
Labeler bryant ranch prepack
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

dextroamphetamine sulfate 5 mg/5mL

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2043
Product ID 72162-2043_9dcba5a8-b4ee-4e3c-a0be-3587072a4c5a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203644
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2013-05-31

Pharmacologic Class

Classes
central nervous system stimulant [epc] central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622043
Hyphenated Format 72162-2043

Supplemental Identifiers

RxCUI
884522
UNII
JJ768O327N

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 (source: ndc)
Generic Name dextroamphetamine (source: ndc)
Application Number ANDA203644 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (72162-2043-2)
source: ndc

Packages (1)

Ingredients (1)

dextroamphetamine sulfate (5 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9dcba5a8-b4ee-4e3c-a0be-3587072a4c5a", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["884522"], "spl_set_id": ["76da9845-2ce1-49a5-9bf3-6a550d623172"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (72162-2043-2)", "package_ndc": "72162-2043-2", "marketing_start_date": "20240403"}], "brand_name": "Dextroamphetamine", "product_id": "72162-2043_9dcba5a8-b4ee-4e3c-a0be-3587072a4c5a", "dosage_form": "SOLUTION", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2043", "dea_schedule": "CII", "generic_name": "Dextroamphetamine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "5 mg/5mL"}], "application_number": "ANDA203644", "marketing_category": "ANDA", "marketing_start_date": "20130531", "listing_expiration_date": "20261231"}