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Cromolyn Sodium
Cromolyn Sodium - 54868-3555-1 - (cromolyn sodium)
Drug Information of Cromolyn Sodium
| Product NDC: | 54868-3555 |
| Proprietary Name: | Cromolyn Sodium |
| Non Proprietary Name: | cromolyn sodium |
| Active Ingredient(s): | 20 mg/2mL & nbsp; cromolyn sodium |
| Administration Route(s): | INTRABRONCHIAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cromolyn Sodium
| Product NDC: | 54868-3555 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075271 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030324 |
Package Information of Cromolyn Sodium
| Package NDC: | 54868-3555-1 |
| Package Description: | 120 VIAL in 1 CARTON (54868-3555-1) > 2 mL in 1 VIAL |
NDC Information of Cromolyn Sodium
| NDC Code | 54868-3555-1 |
| Proprietary Name | Cromolyn Sodium |
| Package Description | 120 VIAL in 1 CARTON (54868-3555-1) > 2 mL in 1 VIAL |
| Product NDC | 54868-3555 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cromolyn sodium |
| Dosage Form Name | SOLUTION |
| Route Name | INTRABRONCHIAL |
| Start Marketing Date | 20030324 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | CROMOLYN SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
