zinc sulfate
NDC 70771-1850, zinc sulfate, injection, solution, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1850
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217074
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1850 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ZINC SULFATE5 mg/mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1850-7 | 70771185007 | 25 VIAL in 1 CARTON (70771-1850-7) / 5 mL in 1 VIAL (70771-1850-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/74d8d07b-cfd9-4262-b689-fea12673bbd1
Use it
Look up 70771-1850 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1850 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1850. 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.