AMPHETAMINE SULFATE
NDC 71335-2990, amphetamine sulfate, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-2990
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212901
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2990 \ -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 |
|---|---|---|
| 71335-2990-1 | 71335299001 | 120 TABLET in 1 BOTTLE (71335-2990-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9817a519-fdb0-474a-92f4-2e485c9cb047
Use it
Look up 71335-2990 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2990 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2990. 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.