OLPRUVA is a Oral Kit in the Human Prescription Drug category. It is labeled and distributed by Acer Therapeutics Inc.. The primary component is .
Product ID | 72542-200_f3b1222e-c8f1-46a8-b0d6-9f57107f6be1 |
NDC | 72542-200 |
Product Type | Human Prescription Drug |
Proprietary Name | OLPRUVA |
Generic Name | Sodium Phenylbutyrate |
Dosage Form | Kit |
Route of Administration | ORAL |
Marketing Start Date | 2022-12-22 |
Marketing Category | NDA / |
Application Number | NDA214860 |
Labeler Name | Acer Therapeutics Inc. |
Active Ingredient Strength | 0 |
NDC Exclude Flag | N |
Listing Certified Through | 2024-12-31 |
Marketing Start Date | 2022-12-22 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
72542-200 | OLPRUVA | sodium phenylbutyrate |
72542-300 | OLPRUVA | sodium phenylbutyrate |
72542-400 | OLPRUVA | sodium phenylbutyrate |
72542-500 | OLPRUVA | sodium phenylbutyrate |
72542-600 | OLPRUVA | sodium phenylbutyrate |
72542-667 | OLPRUVA | sodium phenylbutyrate |
75987-060 | BUPHENYL | sodium phenylbutyrate |
75987-070 | Buphenyl | sodium phenylbutyrate |
71770-100 | PHEBURANE | Sodium phenylbutyrate |
71770-200 | PHEBURANE | Sodium phenylbutyrate |
71770-210 | PHEBURANE | Sodium phenylbutyrate |
42794-086 | Sodium Phenylbutyrate | Sodium Phenylbutyrate |
49884-006 | Sodium Phenylbutyrate | Sodium Phenylbutyrate |
68462-853 | sodium phenylbutyrate | sodium phenylbutyrate |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OLPRUVA 88814846 not registered Live/Pending |
Acer Therapeutics Inc. 2020-02-28 |