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NDC 57844-112, Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate, tablet, from Teva Pharmaceuticals USA, Inc..

Product NDC
57844-112
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040422
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57844-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXTROAMPHETAMINE SACCHARATE3.125 mg/1
  • AMPHETAMINE ASPARTATE MONOHYDRATE3.125 mg/1
  • DEXTROAMPHETAMINE SULFATE3.125 mg/1
  • AMPHETAMINE SULFATE3.125 mg/1

Pharmacologic classes

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]

Package NDCNDC-11Package
57844-112-0157844011201100 TABLET in 1 BOTTLE (57844-112-01)

Linked data

RxNorm, label and prices

Use it

Look up 57844-112 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57844-112 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57844-112. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.