| Product NDC: | 59779-075 | 
| 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: | 59779-075 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA075702 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20010703 | 
| Package NDC: | 59779-075-13 | 
| Package Description: | 1 BOTTLE in 1 CARTON (59779-075-13) > 26 mL in 1 BOTTLE | 
| NDC Code | 59779-075-13 | 
| Proprietary Name | Cromolyn Sodium | 
| Package Description | 1 BOTTLE in 1 CARTON (59779-075-13) > 26 mL in 1 BOTTLE | 
| Product NDC | 59779-075 | 
| 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 | CVS Pharmacy | 
| Substance Name | CROMOLYN SODIUM | 
| Strength Number | 5.2 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes |