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Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate

NDC 57664-642, Dextroamphetamine saccharate, Amphetamine aspartate, Dextroamphetamine sulfate, and Amphetamine sulfate, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
57664-642
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040480
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-642 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXTROAMPHETAMINE SACCHARATE1.875 mg/1
  • AMPHETAMINE ASPARTATE1.875 mg/1
  • DEXTROAMPHETAMINE SULFATE1.875 mg/1
  • AMPHETAMINE SULFATE1.875 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
57664-642-0857664064208100 TABLET in 1 BOTTLE, PLASTIC (57664-642-08)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9af67219-9b37-45d0-ac52-647cbfacd296

Use it

Look up 57664-642 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-642 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-642. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.