Bepreve is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is Bepotastine Besylate.
Product ID | 24208-629_00627586-e9cc-4975-a309-eba6cf8d7d41 |
NDC | 24208-629 |
Product Type | Human Prescription Drug |
Proprietary Name | Bepreve |
Generic Name | Bepotastine Besilate |
Dosage Form | Solution/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 2009-09-08 |
Marketing Category | NDA / NDA |
Application Number | NDA022288 |
Labeler Name | Bausch & Lomb Incorporated |
Substance Name | BEPOTASTINE BESYLATE |
Active Ingredient Strength | 15 mg/mL |
Pharm Classes | Histamine-1 Receptor Antagonist [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2009-09-08 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA022288 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-08 |
Marketing Category | NDA |
Application Number | NDA022288 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2009-09-08 |
Marketing Category | NDA |
Application Number | NDA022288 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2009-09-08 |
Ingredient | Strength |
---|---|
BEPOTASTINE BESILATE | 15 mg/mL |
SPL SET ID: | 68bbf6a0-c4b5-47c1-8a1c-08220fbdbce6 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
24208-629 | Bepreve | bepotastine besilate |
0378-7055 | Bepotastine Besilate | Bepotastine Besilate |
24208-630 | Bepotastine Besilate | bepotastine besilate |
60505-6111 | Bepotastine Besilate | Bepotastine Besilate |
82260-630 | Bepotastine Besilate | bepotastine besilate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BEPREVE 77318560 3722934 Live/Registered |
BAUSCH & LOMB INCORPORATED 2007-10-31 |