Home
>
National Drug Code (NDC)
>
ALAMAST
ALAMAST - 68669-711-10 - (pemirolast potassium)
Drug Information of ALAMAST
| Product NDC: | 68669-711 |
| Proprietary Name: | ALAMAST |
| Non Proprietary Name: | pemirolast potassium |
| Active Ingredient(s): | 1 mg/mL & nbsp; pemirolast potassium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALAMAST
| Product NDC: | 68669-711 |
| Labeler Name: | Vistakon Pharmaceuticals LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021079 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000501 |
Package Information of ALAMAST
| Package NDC: | 68669-711-10 |
| Package Description: | 10 mL in 1 BOTTLE (68669-711-10) |
NDC Information of ALAMAST
| NDC Code | 68669-711-10 |
| Proprietary Name | ALAMAST |
| Package Description | 10 mL in 1 BOTTLE (68669-711-10) |
| Product NDC | 68669-711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pemirolast potassium |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20000501 |
| Marketing Category Name | NDA |
| Labeler Name | Vistakon Pharmaceuticals LLC |
| Substance Name | PEMIROLAST POTASSIUM |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
