Cromolyn Sodium 16571-0600
Product NDC
16571-0600- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Solution, Concentrate
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 5, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA202583
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Cromolyn Sodium | 100 mg/5mL |
Drug Class
Decreased Histamine Release [PE]Mast Cell Stabilizer [EPC]
Packaging Options(1)
12 POUCH in 1 CARTON (16571-600-96) / 8 AMPULE in 1 POUCH / 5 mL in 1 AMPULE