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Cromolyn Sodium
Cromolyn Sodium - 66993-470-96 - (Cromolyn Sodium)
Drug Information of Cromolyn Sodium
| Product NDC: | 66993-470 |
| Proprietary Name: | Cromolyn Sodium |
| 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) |
Labeler Information of Cromolyn Sodium
| Product NDC: | 66993-470 |
| Labeler Name: | Prasco Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020479 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20111212 |
Package Information of Cromolyn Sodium
| Package NDC: | 66993-470-96 |
| Package Description: | 12 POUCH in 1 CARTON (66993-470-96) > 8 AMPULE in 1 POUCH > 5 mL in 1 AMPULE |
NDC Information of Cromolyn Sodium
| NDC Code | 66993-470-96 |
| Proprietary Name | Cromolyn Sodium |
| Package Description | 12 POUCH in 1 CARTON (66993-470-96) > 8 AMPULE in 1 POUCH > 5 mL in 1 AMPULE |
| Product NDC | 66993-470 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cromolyn Sodium |
| Dosage Form Name | SOLUTION, CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 20111212 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Prasco Laboratories |
| Substance Name | CROMOLYN SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
