Home
>
National Drug Code (NDC)
>
Cromolyn Sodium
Cromolyn Sodium - 0172-6406-49 - (Cromolyn Sodium)
Drug Information of Cromolyn Sodium
| Product NDC: | 0172-6406 |
| 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: | 0172-6406 |
| Labeler Name: | IVAX Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075271 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000118 |
Package Information of Cromolyn Sodium
| Package NDC: | 0172-6406-49 |
| Package Description: | 60 VIAL, SINGLE-DOSE in 1 CARTON (0172-6406-49) > 2 mL in 1 VIAL, SINGLE-DOSE (0172-6406-05) |
NDC Information of Cromolyn Sodium
| NDC Code | 0172-6406-49 |
| Proprietary Name | Cromolyn Sodium |
| Package Description | 60 VIAL, SINGLE-DOSE in 1 CARTON (0172-6406-49) > 2 mL in 1 VIAL, SINGLE-DOSE (0172-6406-05) |
| Product NDC | 0172-6406 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cromolyn Sodium |
| Dosage Form Name | SOLUTION |
| Route Name | INTRABRONCHIAL |
| Start Marketing Date | 20000118 |
| Marketing Category Name | ANDA |
| Labeler Name | IVAX Pharmaceuticals, Inc. |
| Substance Name | CROMOLYN SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
