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Cromolyn Sodium

NDC 0172-6406, Cromolyn Sodium, solution, from Teva Pharmaceuticals USA, Inc..

Product NDC
0172-6406
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
SOLUTION
Route
INTRABRONCHIAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075271
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0172-6406 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CROMOLYN SODIUM20 mg/2mL

Pharmacologic classes

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

Package NDCNDC-11Package
0172-6406-490017264064912 POUCH in 1 CARTON (0172-6406-49) / 5 VIAL, SINGLE-DOSE in 1 POUCH (0172-6406-05) / 2 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8fe37a7a-edd6-4733-bb7e-e01c1906aeba

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0172-6406

  • NADAC price for package 00172640649

    GET /v1/drugs/nadac/00172640649

Use it

Look up 0172-6406 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0172-6406 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0172-6406. 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.