Product NDC: | 18860-678 |
Proprietary Name: | Gastrocrom |
Non Proprietary Name: | cromolyn sodium |
Active Ingredient(s): | 20 mg/mL & nbsp; cromolyn sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 18860-678 |
Labeler Name: | Jazz Pharmaceuticals Commercial Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020479 |
Marketing Category: | NDA |
Start Marketing Date: | 19961101 |
Package NDC: | 18860-678-70 |
Package Description: | 12 POUCH in 1 CARTON (18860-678-70) > 8 AMPULE in 1 POUCH > 5 mL in 1 AMPULE |
NDC Code | 18860-678-70 |
Proprietary Name | Gastrocrom |
Package Description | 12 POUCH in 1 CARTON (18860-678-70) > 8 AMPULE in 1 POUCH > 5 mL in 1 AMPULE |
Product NDC | 18860-678 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | cromolyn sodium |
Dosage Form Name | SOLUTION, CONCENTRATE |
Route Name | ORAL |
Start Marketing Date | 19961101 |
Marketing Category Name | NDA |
Labeler Name | Jazz Pharmaceuticals Commercial Corp. |
Substance Name | CROMOLYN SODIUM |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |