Amphetamine Sulfate
NDC 52536-059, Amphetamine Sulfate, tablet, from Wilshire Pharmaceuticals, Inc..
- Product NDC
- 52536-059
- Status
- Listed
- Labeler
- Wilshire Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA200166
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/52536-059 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 52536-059-03 | 52536005903 | 30 TABLET in 1 BOTTLE (52536-059-03) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/91add2e3-8359-47dc-b79f-197d36b02819NADAC price for package 52536005903
GET /v1/drugs/nadac/52536005903
Use it
Look up 52536-059 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/52536-059 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 52536-059. 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.