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Amphetamine Sulfate

NDC 70010-041, Amphetamine Sulfate, tablet, from Granules Pharmaceuticals Inc..

Product NDC
70010-041
Status
Listed
Labeler
Granules Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212619
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70010-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMPHETAMINE SULFATE10 mg/1

Pharmacologic classes

Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]

Package NDCNDC-11Package
70010-041-0170010004101100 TABLET in 1 BOTTLE (70010-041-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/26dbad66-13c4-4906-88b3-ab7ee191466c

  • NADAC price for package 70010004101

    GET /v1/drugs/nadac/70010004101

Use it

Look up 70010-041 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70010-041 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70010-041. 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.