Product NDC: | 37205-223 |
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) |
Product NDC: | 37205-223 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075702 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100703 |
Package NDC: | 37205-223-61 |
Package Description: | 1 BOTTLE in 1 CARTON (37205-223-61) > 26 mL in 1 BOTTLE |
NDC Code | 37205-223-61 |
Proprietary Name | Cromolyn Sodium |
Package Description | 1 BOTTLE in 1 CARTON (37205-223-61) > 26 mL in 1 BOTTLE |
Product NDC | 37205-223 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Cromolyn Sodium |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20100703 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | CROMOLYN SODIUM |
Strength Number | 5.2 |
Strength Unit | mg/mL |
Pharmaceutical Classes |