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  |