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NDC 50633-920, Potassium iodide, tablet, from BTG International Inc.

Product NDC
50633-920
Status
Listed
Labeler
BTG International Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA076350
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50633-920 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • POTASSIUM IODIDE130 mg/1
Package NDCNDC-11Package
50633-920-2050633092020420 BOX in 1 CARTON (50633-920-20) / 20 BLISTER PACK in 1 BOX / 1 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 50633-920 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50633-920 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50633-920. 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.