Home
>
National Drug Code (NDC)
>
ALOCRIL
ALOCRIL - 0023-8842-05 - (nedocromil sodium)
Drug Information of ALOCRIL
| Product NDC: | 0023-8842 |
| Proprietary Name: | ALOCRIL |
| 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 ALOCRIL
| Product NDC: | 0023-8842 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021009 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000203 |
Package Information of ALOCRIL
| Package NDC: | 0023-8842-05 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0023-8842-05) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of ALOCRIL
| NDC Code | 0023-8842-05 |
| Proprietary Name | ALOCRIL |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0023-8842-05) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 0023-8842 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nedocromil sodium |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20000203 |
| Marketing Category Name | NDA |
| Labeler Name | Allergan, Inc. |
| Substance Name | NEDOCROMIL SODIUM |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
