Amoxicillin
NDC 70518-4522, Amoxicillin, powder, for suspension, from REMEDYREPACK INC..
- Product NDC
- 70518-4522
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA065334
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4522 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AMOXICILLIN400 mg/5mL
Pharmacologic classes
Penicillin-class Antibacterial [EPC]; Penicillins [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-4522-0 | 70518452200 | 100 mL in 1 BOTTLE (70518-4522-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2732a8c7-9e4b-43c9-9712-df4b237ab69c
Use it
Look up 70518-4522 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4522 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4522. 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.