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Betimol
Betimol - 68669-525-99 - (timolol)
Drug Information of Betimol
| Product NDC: | 68669-525 |
| Proprietary Name: | Betimol |
| Non Proprietary Name: | timolol |
| Active Ingredient(s): | 5 mg/mL & nbsp; timolol |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Betimol
| Product NDC: | 68669-525 |
| Labeler Name: | Vistakon Pharmaceuticals LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020439 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20001001 |
Package Information of Betimol
| Package NDC: | 68669-525-99 |
| Package Description: | 2.5 mL in 1 BOTTLE (68669-525-99) |
NDC Information of Betimol
| NDC Code | 68669-525-99 |
| Proprietary Name | Betimol |
| Package Description | 2.5 mL in 1 BOTTLE (68669-525-99) |
| Product NDC | 68669-525 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | timolol |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20001001 |
| Marketing Category Name | NDA |
| Labeler Name | Vistakon Pharmaceuticals LLC |
| Substance Name | TIMOLOL |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
