Pred-Brom is a Ophthalmic Suspension/ Drops in the Human Prescription Drug category. It is labeled and distributed by Imprimis Njof, Llc. The primary component is Prednisolone Acetate; Bromfenac Sodium.
Product ID | 71384-505_632b3f47-ae7c-3e64-e053-2991aa0a59f9 |
NDC | 71384-505 |
Product Type | Human Prescription Drug |
Proprietary Name | Pred-Brom |
Generic Name | Prednisolone Acetate-bromfenac |
Dosage Form | Suspension/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 2018-01-05 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Imprimis NJOF, LLC |
Substance Name | PREDNISOLONE ACETATE; BROMFENAC SODIUM |
Active Ingredient Strength | 10 mg/mL; mg/mL |
Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2018-01-05 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2018-01-05 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
PREDNISOLONE ACETATE | 10 mg/mL |
SPL SET ID: | 63254869-67d5-0900-e053-2a91aa0af95c |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
70261-505 | Pred-Brom | Prednisolone Acetate-Bromfenac |
71384-505 | Pred-Brom | Prednisolone Acetate-Bromfenac |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRED-BROM 87731119 5577593 Live/Registered |
HARROW IP, LLC 2017-12-21 |