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ALOMIDE
ALOMIDE - 0065-0345-10 - (lodoxamide tromethamine)
Drug Information of ALOMIDE
| Product NDC: | 0065-0345 |
| Proprietary Name: | ALOMIDE |
| Non Proprietary Name: | lodoxamide tromethamine |
| Active Ingredient(s): | 1.78 mg/mL & nbsp; lodoxamide tromethamine |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ALOMIDE
| Product NDC: | 0065-0345 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020191 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930930 |
Package Information of ALOMIDE
| Package NDC: | 0065-0345-10 |
| Package Description: | 10 mL in 1 BOTTLE, PLASTIC (0065-0345-10) |
NDC Information of ALOMIDE
| NDC Code | 0065-0345-10 |
| Proprietary Name | ALOMIDE |
| Package Description | 10 mL in 1 BOTTLE, PLASTIC (0065-0345-10) |
| Product NDC | 0065-0345 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lodoxamide tromethamine |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19930930 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | LODOXAMIDE TROMETHAMINE |
| Strength Number | 1.78 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Decreased Histamine Release [PE],Mast Cell Stabilizer [EPC] |
