CROMOLYN SODIUM
NDC 16571-600, CROMOLYN SODIUM, solution, concentrate, from Rising Pharma Holdings, Inc..
- Product NDC
- 16571-600
- Status
- Listed
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- SOLUTION, CONCENTRATE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202583
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/16571-600 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 16571-600-96 | 16571060096 | 12 POUCH in 1 CARTON (16571-600-96) / 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/61c9cb85-129e-4490-b5f7-357307fcecbfNADAC price for package 16571060096
GET /v1/drugs/nadac/16571060096
Use it
Look up 16571-600 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/16571-600 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 16571-600. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.