Dextroamphetamine Sulfate
NDC 27808-090, Dextroamphetamine Sulfate, tablet, from Cranbury Pharmaceuticals, LLC.
- Product NDC
- 27808-090
- Status
- Listed
- Labeler
- Cranbury Pharmaceuticals, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206095
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/27808-090 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DEXTROAMPHETAMINE SULFATE10 mg/1
Pharmacologic classes
Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 27808-090-01 | 27808009001 | 100 TABLET in 1 BOTTLE, PLASTIC (27808-090-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9acdf000-fefe-47c7-a44c-0f7a65c5c05c
Use it
Look up 27808-090 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/27808-090 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 27808-090. 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.