Amoxicillin
NDC 42708-112, Amoxicillin, tablet, film coated, from QPharma, Inc..
- Product NDC
- 42708-112
- Status
- Listed
- Labeler
- QPharma, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA065056
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42708-112 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AMOXICILLIN875 mg/1
Pharmacologic classes
Penicillin-class Antibacterial [EPC]; Penicillins [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42708-112-20 | 42708011220 | 20 TABLET, FILM COATED in 1 BOTTLE (42708-112-20) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7f40b439-d826-4a19-b184-702e9bd5a883
Use it
Look up 42708-112 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42708-112 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42708-112. 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.