Allopurinol
NDC 70771-1127, Allopurinol, tablet, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1127
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210117
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1127 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALLOPURINOL300 mg/1
Pharmacologic classes
Xanthine Oxidase Inhibitor [EPC]; Xanthine Oxidase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1127-0 | 70771112700 | 1000 TABLET in 1 BOTTLE (70771-1127-0) |
| 70771-1127-1 | 70771112701 | 100 TABLET in 1 BOTTLE (70771-1127-1) |
| 70771-1127-5 | 70771112705 | 500 TABLET in 1 BOTTLE (70771-1127-5) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9232f484-a5f6-4c63-b7f4-b510d2827159
Use it
Look up 70771-1127 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1127 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1127. 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.