| 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] |