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NDC 55259-1191, oyster shell, tablet, from APEXEL CO., LTD..

Product NDC
55259-1191
Status
Listed
Labeler
APEXEL CO., LTD.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55259-1191 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OSTREA EDULIS SHELL.67 mg/1
Package NDCNDC-11Package
55259-1191-155259119101120 TABLET in 1 BOTTLE (55259-1191-1)

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 55259-1191 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55259-1191 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55259-1191. 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.