Prolate is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Forte Bio-pharma Llc. The primary component is Oxycodone Hydrochloride; Acetaminophen.
| Product ID | 72245-682_9cbc4097-efc7-9042-e053-2995a90a060c |
| NDC | 72245-682 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Prolate |
| Generic Name | Oxycodone And Acetaminophen |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2020-02-17 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA040608 |
| Labeler Name | Forte Bio-Pharma LLC |
| Substance Name | OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN |
| Active Ingredient Strength | 8 mg/1; mg/1 |
| Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule | CII |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2020-02-17 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA040608 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2020-02-17 |
| Marketing Category | ANDA |
| Application Number | ANDA040608 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2020-02-17 |
| Ingredient | Strength |
|---|---|
| OXYCODONE HYDROCHLORIDE | 7.5 mg/1 |
| SPL SET ID: | 9cbbfa94-37b9-9652-e053-2995a90a736b |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 72245-681 | Prolate | Prolate |
| 72245-682 | Prolate | Prolate |
| 72245-683 | Prolate | Prolate |
| 72245-648 | Prolate | Prolate |
| 0054-0551 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 0228-2981 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 0228-2982 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 0228-2983 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 0527-1669 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 0527-1671 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 0904-7093 | OXYCODONE AND ACETAMINOPHEN | oxycodone and acetaminophen |
| 0904-7094 | OXYCODONE AND ACETAMINOPHEN | oxycodone and acetaminophen |
| 0904-7095 | OXYCODONE AND ACETAMINOPHEN | oxycodone and acetaminophen |
| 10544-621 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 10702-184 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 10702-185 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 10702-186 | Oxycodone and Acetaminophen | Oxycodone and Acetaminophen |
| 0054-3686 | Roxicet | Oxycodone and Acetaminophen |
| 0054-4650 | Roxicet | Oxycodone and Acetaminophen |
| 0054-8648 | Roxicet | Oxycodone and Acetaminophen |
| 0054-8650 | Roxicet | Oxycodone and Acetaminophen |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PROLATE 88695547 not registered Live/Pending |
Argent Development Group, LLC 2019-11-17 |
![]() PROLATE 87035226 not registered Live/Pending |
Argent Development Group, LLC 2016-05-12 |
![]() PROLATE 85773194 not registered Dead/Abandoned |
Argent Development Group, LLC 2012-11-06 |
![]() PROLATE 72165639 0787384 Dead/Expired |
STAUFFER CHEMICAL COMPANY 1963-03-28 |