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Zinc sulfate

NDC 70069-692, Zinc sulfate, solution, from Somerset Therapeutics, LLC.

Product NDC
70069-692
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216135
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-692 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZINC SULFATE3 mg/mL

Pharmacologic classes

Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]

Package NDCNDC-11Package
70069-692-257006906922525 VIAL in 1 CARTON (70069-692-25) / 10 mL in 1 VIAL (70069-692-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c9d45d0e-a165-4112-81f9-c0e455572ecf

Use it

Look up 70069-692 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-692 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-692. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.