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Cromolyn Sodium

NDC 71205-230, Cromolyn Sodium, solution/ drops, from Proficient Rx LP.

Product NDC
71205-230
Status
Listed
Labeler
Proficient Rx LP
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075282
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CROMOLYN SODIUM40 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
71205-230-107120502301010 mL in 1 BOTTLE, PLASTIC (71205-230-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/34ef00e8-0c01-4225-9a40-822ab245752a

Use it

Look up 71205-230 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-230. 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.