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Bepreve
Bepreve - 24208-629-02 - (bepotastine besilate)
Drug Information of Bepreve
| Product NDC: | 24208-629 |
| Proprietary Name: | Bepreve |
| Non Proprietary Name: | bepotastine besilate |
| Active Ingredient(s): | 15 mg/mL & nbsp; bepotastine besilate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bepreve
| Product NDC: | 24208-629 |
| Labeler Name: | Bausch & Lomb Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022288 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090908 |
Package Information of Bepreve
| Package NDC: | 24208-629-02 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (24208-629-02) > 5 mL in 1 BOTTLE, DROPPER |
NDC Information of Bepreve
| NDC Code | 24208-629-02 |
| Proprietary Name | Bepreve |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-629-02) > 5 mL in 1 BOTTLE, DROPPER |
| Product NDC | 24208-629 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | bepotastine besilate |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20090908 |
| Marketing Category Name | NDA |
| Labeler Name | Bausch & Lomb Incorporated |
| Substance Name | BEPOTASTINE BESILATE |
| Strength Number | 15 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Histamine-1 Receptor Antagonist [EPC] |
