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Cromolyn Sodium
Cromolyn Sodium - 57782-397-26 - (Cromolyn Sodium)
Drug Information of Cromolyn Sodium
| Product NDC: | 57782-397 |
| Proprietary Name: | Cromolyn Sodium |
| Non Proprietary Name: | Cromolyn Sodium |
| Active Ingredient(s): | 5.2 mg/mL & nbsp; Cromolyn Sodium |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cromolyn Sodium
| Product NDC: | 57782-397 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075702 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010703 |
Package Information of Cromolyn Sodium
| Package NDC: | 57782-397-26 |
| Package Description: | 1 BOTTLE in 1 CARTON (57782-397-26) > 26 mL in 1 BOTTLE |
NDC Information of Cromolyn Sodium
| NDC Code | 57782-397-26 |
| Proprietary Name | Cromolyn Sodium |
| Package Description | 1 BOTTLE in 1 CARTON (57782-397-26) > 26 mL in 1 BOTTLE |
| Product NDC | 57782-397 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cromolyn Sodium |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20010703 |
| Marketing Category Name | ANDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | CROMOLYN SODIUM |
| Strength Number | 5.2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
