Home
>
National Drug Code (NDC)
>
Nedocromil Sodium
Nedocromil Sodium - 17478-066-10 - (Nedocromil Sodium)
Drug Information of Nedocromil Sodium
| Product NDC: | 17478-066 |
| Proprietary Name: | Nedocromil Sodium |
| Non Proprietary Name: | Nedocromil Sodium |
| Active Ingredient(s): | 20 mg/mL & nbsp; Nedocromil Sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nedocromil Sodium
| Product NDC: | 17478-066 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090638 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120910 |
Package Information of Nedocromil Sodium
| Package NDC: | 17478-066-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (17478-066-10) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of Nedocromil Sodium
| NDC Code | 17478-066-10 |
| Proprietary Name | Nedocromil Sodium |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (17478-066-10) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 17478-066 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nedocromil Sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20120910 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | NEDOCROMIL SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
