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CROMOLYN SODIUM

NDC 81665-104, CROMOLYN SODIUM, solution, concentrate, from Omnivium Pharmaceuticals LLC.

Product NDC
81665-104
Status
Listed
Labeler
Omnivium Pharmaceuticals LLC
Dosage form
SOLUTION, CONCENTRATE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209264
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/81665-104 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CROMOLYN SODIUM100 mg/5mL

Pharmacologic classes

Decreased Histamine Release [PE]; Mast Cell Stabilizer [EPC]

Package NDCNDC-11Package
81665-104-968166501049612 POUCH in 1 CARTON (81665-104-96) / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a742664b-265e-49f9-9744-d04e1fb620ae

  • NADAC price for package 81665010496

    GET /v1/drugs/nadac/81665010496

Use it

Look up 81665-104 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81665-104 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81665-104. 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.