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DUREZOL
DUREZOL - 0065-9240-07 - (DUREZOL)
Drug Information of DUREZOL
| Product NDC: | 0065-9240 |
| Proprietary Name: | DUREZOL |
| Non Proprietary Name: | DUREZOL |
| Active Ingredient(s): | .5 mg/mL & nbsp; DUREZOL |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DUREZOL
| Product NDC: | 0065-9240 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022212 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110125 |
Package Information of DUREZOL
| Package NDC: | 0065-9240-07 |
| Package Description: | 5 mL in 1 BOTTLE (0065-9240-07) |
NDC Information of DUREZOL
| NDC Code | 0065-9240-07 |
| Proprietary Name | DUREZOL |
| Package Description | 5 mL in 1 BOTTLE (0065-9240-07) |
| Product NDC | 0065-9240 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DUREZOL |
| Dosage Form Name | EMULSION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110125 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | DIFLUPREDNATE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
