Ketoprofen is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Ketoprofen.
| Product ID | 63629-3642_d30a0ce3-e747-448a-98ab-6b5804003061 |
| NDC | 63629-3642 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Ketoprofen |
| Generic Name | Ketoprofen |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 1993-01-01 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA073516 |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | KETOPROFEN |
| Active Ingredient Strength | 50 mg/1 |
| Pharm Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1993-01-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA073516 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-09-12 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073516 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-09-12 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073516 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-09-12 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073516 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-09-12 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073516 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-09-12 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073516 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-09-12 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073516 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-09-12 |
| Marketing End Date | 2017-12-31 |
| Ingredient | Strength |
|---|---|
| KETOPROFEN | 50 mg/1 |
| SPL SET ID: | 79f475c8-f978-c0ee-b900-f270b59c492d |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| PHarm Class EPC | |
| NUI Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0276-0504 | Ketoprofen | Ketoprofen |
| 0276-0506 | Ketoprofen | Ketoprofen |
| 0378-8200 | Ketoprofen | ketoprofen |
| 21695-340 | Ketoprofen | ketoprofen |
| 21695-341 | Ketoprofen | ketoprofen |
| 23155-020 | ketoprofen | ketoprofen |
| 23155-021 | ketoprofen | ketoprofen |
| 23155-022 | ketoprofen | ketoprofen |
| 33261-064 | Ketoprofen | Ketoprofen |
| 42254-037 | Ketoprofen | Ketoprofen |
| 43063-737 | Ketoprofen | Ketoprofen |
| 45865-379 | Ketoprofen | Ketoprofen |
| 45865-485 | Ketoprofen | Ketoprofen |
| 50090-2729 | Ketoprofen | Ketoprofen |
| 52959-245 | Ketoprofen | Ketoprofen |
| 53217-221 | Ketoprofen | Ketoprofen |
| 63187-018 | Ketoprofen | Ketoprofen |
| 63629-1836 | Ketoprofen | Ketoprofen |
| 63629-3642 | Ketoprofen | Ketoprofen |
| 66267-126 | Ketoprofen | Ketoprofen |
| 67296-0369 | Ketoprofen | Ketoprofen |
| 68788-6400 | Ketoprofen | Ketoprofen |
| 68788-9088 | Ketoprofen | Ketoprofen |
| 69336-127 | Ketoprofen | Ketoprofen |