Allopurinol
NDC 43063-975, Allopurinol, tablet, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 43063-975
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA071450
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/43063-975 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALLOPURINOL100 mg/1
Pharmacologic classes
Xanthine Oxidase Inhibitor [EPC]; Xanthine Oxidase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 43063-975-20 | 43063097520 | 20 TABLET in 1 BOTTLE, PLASTIC (43063-975-20) |
| 43063-975-90 | 43063097590 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-975-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b2ab2389-ccaf-487b-9985-50e3539e7617
Use it
Look up 43063-975 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43063-975 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43063-975. 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.