Home
>
National Drug Code (NDC)
>
NasalCrom
NasalCrom - 52183-199-14 - (cromolyn sodium)
Drug Information of NasalCrom
| Product NDC: | 52183-199 |
| Proprietary Name: | NasalCrom |
| Non Proprietary Name: | cromolyn sodium |
| Active Ingredient(s): | 5.2 mg/1 & nbsp; cromolyn sodium |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NasalCrom
| Product NDC: | 52183-199 |
| Labeler Name: | Prestige Brands Holdings, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075702 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091029 |
Package Information of NasalCrom
| Package NDC: | 52183-199-14 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (52183-199-14) > 100 SPRAY, METERED in 1 BOTTLE, PUMP |
NDC Information of NasalCrom
| NDC Code | 52183-199-14 |
| Proprietary Name | NasalCrom |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (52183-199-14) > 100 SPRAY, METERED in 1 BOTTLE, PUMP |
| Product NDC | 52183-199 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | cromolyn sodium |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20091029 |
| Marketing Category Name | ANDA |
| Labeler Name | Prestige Brands Holdings, Inc. |
| Substance Name | CROMOLYN SODIUM |
| Strength Number | 5.2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
